SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Linked Data
ClinVar Variation Id:
1066884
ClinVar RCV Id:
RCV001378002
dbSNP Id:
rs2148666907
COSMIC:
COSM4701405
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154032405C>T , CM000685.2:g.154032405C>T | GRCh38 |
| NC_000023.10:g.153297856C>T , CM000685.1:g.153297856C>T | GRCh37 |
| NC_000023.9:g.152951050C>T | NCBI36 |
| NG_007107.2:g.109723G>A | |
| NG_007107.3:g.109699G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303391.11:c.179G>A MANE Plus Clinical | ENSP00000301948.6:p.Gly60Asp | |
| ENST00000453960.7:c.215G>A MANE Select | ENSP00000395535.2:p.Gly72Asp | |
| ENST00000303391.10:c.179G>A | ENSP00000301948.6:p.Gly60Asp | |
| ENST00000369957.5:c.*233G>A | ENSP00000358973.4:n.*233G>A | |
| ENST00000407218.5:c.215G>A | ENSP00000384865.2:p.Gly72Asp | |
| ENST00000453960.6:c.215G>A | ENSP00000395535.2:p.Gly72Asp | |
| ENST00000486506.5:n.2527G>A | ||
| ENST00000496908.5:n.310G>A | ||
| ENST00000611468.1:c.167G>A | ENSP00000479736.1:p.Gly56Asp | |
| ENST00000619732.4:c.179G>A | ENSP00000480973.1:p.Gly60Asp | |
| ENST00000622433.4:c.167G>A | ENSP00000484470.1:p.Gly56Asp | |
| ENST00000628176.2:c.179G>A | ENSP00000486978.1:p.Gly60Asp | |
| ENST00000631210.1:n.458G>A | ||
| NM_001110792.1:c.215G>A | NP_001104262.1:p.Gly72Asp | |
| NM_001316337.1:c.-101G>A | NP_001303266.1:n.-101G>A | |
| NM_004992.3:c.179G>A | NP_004983.1:p.Gly60Asp | |
| XM_005274681.3:c.179G>A | XP_005274738.1:p.Gly60Asp | |
| XM_005274682.3:c.-101G>A | XP_005274739.1:n.-101G>A | |
| XM_005274683.3:c.-101G>A | XP_005274740.1:n.-101G>A | |
| XM_011531166.1:c.-101G>A | XP_011529468.1:n.-101G>A | |
| XM_006724819.3:c.-382G>A | XP_006724882.1:n.-382G>A | |
| XM_011531166.2:c.-101G>A | XP_011529468.1:n.-101G>A | |
| XM_024452383.1:c.-101G>A | XP_024308151.1:n.-101G>A | |
| XM_024452384.1:c.-101G>A | XP_024308152.1:n.-101G>A | |
| NM_001110792.2:c.215G>A MANE Select | NP_001104262.1:p.Gly72Asp | |
| NM_001316337.2:c.-101G>A | NP_001303266.1:n.-101G>A | |
| NM_001369391.2:c.-101G>A | NP_001356320.1:n.-101G>A | |
| NM_001369392.2:c.-101G>A | NP_001356321.1:n.-101G>A | |
| NM_001369393.2:c.-101G>A | NP_001356322.1:n.-101G>A | |
| NM_001369394.1:c.-101G>A | NP_001356323.1:n.-101G>A | |
| NM_001369394.2:c.-101G>A | NP_001356323.1:n.-101G>A | |
| NM_001386137.1:c.-382G>A | NP_001373066.1:n.-382G>A | |
| NM_001386138.1:c.-382G>A | NP_001373067.1:n.-382G>A | |
| NM_001386139.1:c.-382G>A | NP_001373068.1:n.-382G>A | |
| NM_004992.4:c.179G>A MANE Plus Clinical | NP_004983.1:p.Gly60Asp |