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:
3002247
ClinVar RCV Id:
RCV003865374
MyVariant Identifiers:
chr16:g.23632745A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23621424A>C , CM000678.2:g.23621424A>C | GRCh38 |
| NC_000016.9:g.23632745A>C , CM000678.1:g.23632745A>C | GRCh37 |
| NC_000016.8:g.23540246A>C | NCBI36 |
| NG_007406.1:g.24934T>G , LRG_308:g.24934T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.3057T>G | ENSP00000460666.3:p.Ala1019= | |
| ENST00000565038.2:c.*532T>G | ENSP00000459882.2:n.*532T>G | |
| ENST00000566069.6:c.3051T>G | ENSP00000459237.2:p.Ala1017= | |
| ENST00000697377.2:c.2895T>G | ENSP00000513286.2:p.Ala965= | |
| ENST00000697379.2:c.3057T>G | ENSP00000513287.2:p.Ala1019= | |
| ENST00000561514.2:c.2166T>G | ENSP00000460666.2:p.Ala722= | |
| ENST00000697374.1:c.2166T>G | ENSP00000513284.1:p.Ala722= | |
| ENST00000697375.1:n.4398T>G | ||
| ENST00000697376.1:c.2166T>G | ENSP00000513285.1:p.Ala722= | |
| ENST00000697377.1:c.2004T>G | ENSP00000513286.1:p.Ala668= | |
| ENST00000697378.1:n.3571T>G | ||
| ENST00000697379.1:c.2166T>G | ENSP00000513287.1:p.Ala722= | |
| ENST00000697380.1:n.2343T>G | ||
| ENST00000697381.1:n.1746T>G | ||
| ENST00000697382.1:c.2166T>G | ENSP00000513288.1:p.Ala722= | |
| ENST00000697383.1:c.585T>G | ENSP00000513289.1:p.Ala195= | |
| ENST00000261584.9:c.3051T>G MANE Select | ENSP00000261584.4:p.Ala1017= | |
| ENST00000261584.8:c.3051T>G | ENSP00000261584.4:p.Ala1017= | |
| ENST00000568219.5:c.2166T>G | ENSP00000454703.2:p.Ala722= | |
| NM_024675.3:c.3051T>G , LRG_308t1:c.3051T>G | NP_078951.2:p.Ala1017= | |
| XM_011545946.1:c.3057T>G | XP_011544248.1:p.Ala1019= | |
| XM_011545947.1:c.3057T>G | XP_011544249.1:p.Ala1019= | |
| XM_011545948.1:c.2166T>G | XP_011544250.1:p.Ala722= | |
| XR_950851.1:n.3847T>G | ||
| XM_011545946.2:c.3057T>G | XP_011544248.1:p.Ala1019= | |
| XM_011545947.2:c.3057T>G | XP_011544249.1:p.Ala1019= | |
| XM_011545948.2:c.2166T>G | XP_011544250.1:p.Ala722= | |
| XM_017023671.1:c.3057T>G | XP_016879160.1:p.Ala1019= | |
| XM_017023672.2:c.3051T>G | XP_016879161.1:p.Ala1017= | |
| XM_017023673.2:c.3051T>G | XP_016879162.1:p.Ala1017= | |
| NM_024675.4:c.3051T>G MANE Select | NP_078951.2:p.Ala1017= |