Linked Data
ClinVar Variation Id:
1961599
ClinVar RCV Id:
RCV002720794
dbSNP Id:
rs763116900
ExAC:
7:92135628 T / C
gnomAD v2:
7-92135628-T-C
gnomAD v4:
7-92506314-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92506314T>C , CM000669.2:g.92506314T>C | GRCh38 |
| NC_000007.13:g.92135628T>C , CM000669.1:g.92135628T>C | GRCh37 |
| NC_000007.12:g.91973564T>C | NCBI36 |
| NG_008341.1:g.27218A>G | |
| NG_008341.2:g.27218A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000248633.9:c.1834A>G MANE Select | ENSP00000248633.4:p.Ile612Val | |
| ENST00000248633.8:c.1834A>G | ENSP00000248633.4:p.Ile612Val | |
| ENST00000422866.1:c.652A>G | ||
| ENST00000428214.5:c.1834A>G | ENSP00000394413.1:p.Ile612Val | |
| ENST00000438045.5:c.868A>G | ENSP00000410438.1:p.Ile290Val | |
| ENST00000484913.5:n.1873A>G | ||
| ENST00000496420.5:n.1510A>G | ||
| NM_000466.2:c.1834A>G | NP_000457.1:p.Ile612Val | |
| NM_001282677.1:c.1834A>G | NP_001269606.1:p.Ile612Val | |
| NM_001282678.1:c.1210A>G | NP_001269607.1:p.Ile404Val | |
| XM_005250433.3:c.85A>G | XP_005250490.1:p.Ile29Val | |
| XR_242246.3:n.1930A>G | ||
| XM_017012319.2:c.85A>G | XP_016867808.1:p.Ile29Val | |
| XR_001744808.2:n.861A>G | ||
| XR_242246.5:n.1881A>G | ||
| NM_000466.3:c.1834A>G MANE Select | NP_000457.1:p.Ile612Val | |
| NM_001282677.2:c.1834A>G | NP_001269606.1:p.Ile612Val | |
| NM_001282678.2:c.1210A>G | NP_001269607.1:p.Ile404Val |