Linked Data
ClinVar Variation Id:
2911857
ClinVar RCV Id:
RCV003601341
dbSNP Id:
rs1341607701
gnomAD v2:
17-7127028-C-T
gnomAD v3:
17-7223709-C-T
gnomAD v4:
17-7223709-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7223709C>T , CM000679.2:g.7223709C>T | GRCh38 |
| NC_000017.10:g.7127028C>T , CM000679.1:g.7127028C>T | GRCh37 |
| NC_000017.9:g.7067752C>T | NCBI36 |
| NG_007975.1:g.8876C>T | |
| NG_008391.2:g.1342G>A | |
| NG_033038.1:g.15836G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1248C>T MANE Select | ENSP00000349297.5:p.Ala416= | |
| ENST00000322910.9:c.*1203C>T | ENSP00000325395.5:n.*1203C>T | |
| ENST00000350303.9:c.1182C>T | ENSP00000344152.5:p.Ala394= | |
| ENST00000356839.9:c.1248C>T | ENSP00000349297.5:p.Ala416= | |
| ENST00000542255.6:c.106C>T | ||
| ENST00000543245.6:c.1317C>T | ENSP00000438689.2:p.Ala439= | |
| ENST00000578579.2:n.419C>T | ||
| ENST00000578711.1:n.205C>T | ||
| ENST00000578824.5:n.664C>T | ||
| ENST00000579425.5:n.272C>T | ||
| ENST00000579546.1:c.85C>T | ||
| ENST00000583850.5:n.23C>T | ||
| ENST00000583858.5:c.277C>T | ||
| ENST00000585203.6:n.456C>T | ||
| NM_000018.3:c.1248C>T | NP_000009.1:p.Ala416= | |
| NM_001033859.2:c.1182C>T | NP_001029031.1:p.Ala394= | |
| NM_001270447.1:c.1317C>T | NP_001257376.1:p.Ala439= | |
| NM_001270448.1:c.1020C>T | NP_001257377.1:p.Ala340= | |
| XM_006721516.2:c.1248C>T | XP_006721579.2:p.Ala416= | |
| XM_011523829.1:c.1248C>T | XP_011522131.1:p.Ala416= | |
| XM_011523830.1:c.1248C>T | XP_011522132.1:p.Ala416= | |
| XR_934021.1:n.1355C>T | ||
| XR_934022.1:n.1355C>T | ||
| XR_934023.1:n.1355C>T | ||
| XM_006721516.3:c.1248C>T | XP_006721579.2:p.Ala416= | |
| XM_011523829.2:c.1248C>T | XP_011522131.1:p.Ala416= | |
| XM_011523830.2:c.1248C>T | XP_011522132.1:p.Ala416= | |
| XM_024450741.1:c.1248C>T | XP_024306509.1:p.Ala416= | |
| XR_934021.2:n.1307C>T | ||
| XR_934022.2:n.1307C>T | ||
| XR_934023.2:n.1307C>T | ||
| NM_000018.4:c.1248C>T MANE Select | NP_000009.1:p.Ala416= | |
| NM_001033859.3:c.1182C>T | NP_001029031.1:p.Ala394= | |
| NM_001270447.2:c.1317C>T | NP_001257376.1:p.Ala439= | |
| NM_001270448.2:c.1020C>T | NP_001257377.1:p.Ala340= |