Linked Data
dbSNP Id:
rs774192504
ExAC:
1:64089275 G / A
gnomAD v2:
1-64089275-G-A
gnomAD v4:
1-63623604-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.63623604G>A , CM000663.2:g.63623604G>A | GRCh38 |
| NC_000001.10:g.64089275G>A , CM000663.1:g.64089275G>A | GRCh37 |
| NC_000001.9:g.63861863G>A | NCBI36 |
| NG_016966.1:g.35329G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371084.8:c.247-5821G>A MANE Select | ENSP00000360125.3:n.247-5821G>A | |
| ENST00000650546.1:c.247-5821G>A | ENSP00000497812.1:n.247-5821G>A | |
| ENST00000371083.4:c.144G>A | ENSP00000360124.4:p.Glu48= | |
| ENST00000371084.7:c.247-5821G>A | ENSP00000360125.3:n.247-5821G>A | |
| ENST00000540265.5:c.-345-5821G>A | ENSP00000443449.1:n.-345-5821G>A | |
| NM_001172818.1:c.144G>A | NP_001166289.1:p.Glu48= | |
| NM_001172819.1:c.-345-5821G>A | NP_001166290.1:n.-345-5821G>A | |
| NM_002633.2:c.247-5821G>A | NP_002624.2:n.247-5821G>A | |
| NM_002633.3:c.247-5821G>A MANE Select | NP_002624.2:n.247-5821G>A | |
| NM_001172819.2:c.-345-5821G>A | NP_001166290.1:n.-345-5821G>A |