Linked Data
ClinVar Variation Id:
320071
dbSNP Id:
rs563734833
ExAC:
16:57935474 G / A
gnomAD v2:
16-57935474-G-A
gnomAD v3:
16-57901570-G-A
gnomAD v4:
16-57901570-G-A
COSMIC:
COSM1378609
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.57901570G>A , CM000678.2:g.57901570G>A | GRCh38 |
| NC_000016.9:g.57935474G>A , CM000678.1:g.57935474G>A | GRCh37 |
| NC_000016.8:g.56492975G>A | NCBI36 |
| NG_016351.1:g.74547C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251102.13:c.2850C>T MANE Select | ENSP00000251102.8:p.Ile950= | |
| ENST00000251102.12:c.2850C>T | ENSP00000251102.8:p.Ile950= | |
| ENST00000564448.5:c.2832C>T | ENSP00000454633.1:p.Ile944= | |
| ENST00000569643.1:n.507C>T | ||
| NM_001286130.1:c.2832C>T | NP_001273059.1:p.Ile944= | |
| NM_001297.4:c.2850C>T | NP_001288.3:p.Ile950= | |
| XM_006721134.2:c.2850C>T | XP_006721197.1:p.Ile950= | |
| XM_011522870.1:c.1701C>T | XP_011521172.1:p.Ile567= | |
| XM_011522870.2:c.1701C>T | XP_011521172.1:p.Ile567= | |
| NM_001286130.2:c.2832C>T | NP_001273059.1:p.Ile944= | |
| NM_001297.5:c.2850C>T MANE Select | NP_001288.3:p.Ile950= |