Linked Data
ClinVar Variation Id:
541189
ClinVar RCV Id:
RCV000651398
dbSNP Id:
rs563420866
ExAC:
1:985936 C / T
gnomAD v2:
1-985936-C-T
gnomAD v3:
1-1050556-C-T
gnomAD v4:
1-1050556-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1050556C>T , CM000663.2:g.1050556C>T | GRCh38 |
| NC_000001.10:g.985936C>T , CM000663.1:g.985936C>T | GRCh37 |
| NC_000001.9:g.975799C>T | NCBI36 |
| NG_016346.1:g.35434C>T , LRG_198:g.35434C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379370.7:c.5106C>T MANE Select | ENSP00000368678.2:p.Phe1702= | |
| ENST00000651234.1:c.4791C>T | ENSP00000499046.1:p.Phe1597= | |
| ENST00000652369.1:c.4791C>T | ENSP00000498543.1:p.Phe1597= | |
| ENST00000379370.6:c.5106C>T | ENSP00000368678.2:p.Phe1702= | |
| ENST00000419249.1:c.1C>T | ||
| ENST00000620552.4:c.4692C>T | ENSP00000484607.1:p.Phe1564= | |
| NM_001305275.1:c.5106C>T | NP_001292204.1:p.Phe1702= | |
| NM_198576.3:c.5106C>T | NP_940978.2:p.Phe1702= | |
| XM_005244749.2:c.5106C>T | XP_005244806.1:p.Phe1702= | |
| XM_006710635.2:c.5106C>T | XP_006710698.1:p.Phe1702= | |
| XM_011541429.1:c.5106C>T | XP_011539731.1:p.Phe1702= | |
| XM_011541430.1:c.4233C>T | XP_011539732.1:p.Phe1411= | |
| XM_011541431.1:c.3372C>T | XP_011539733.1:p.Phe1124= | |
| XR_946650.1:n.5173C>T | ||
| NM_001364727.1:c.4791C>T | NP_001351656.1:p.Phe1597= | |
| XM_005244749.3:c.5106C>T | XP_005244806.1:p.Phe1702= | |
| XM_011541429.2:c.5106C>T | XP_011539731.1:p.Phe1702= | |
| XR_946650.2:n.5177C>T | ||
| NM_001305275.2:c.5106C>T | NP_001292204.1:p.Phe1702= | |
| NM_198576.4:c.5106C>T MANE Select | NP_940978.2:p.Phe1702= | |
| NM_001364727.2:c.4791C>T | NP_001351656.1:p.Phe1597= |