Linked Data
dbSNP Id:
rs747960081
ExAC:
1:197062282 G / A
gnomAD v2:
1-197062282-G-A
gnomAD v4:
1-197093152-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197093152G>A , CM000663.2:g.197093152G>A | GRCh38 |
| NC_000001.10:g.197062282G>A , CM000663.1:g.197062282G>A | GRCh37 |
| NC_000001.9:g.195328905G>A | NCBI36 |
| NG_015867.1:g.58543C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367408.6:n.2481C>T | ||
| ENST00000367409.9:c.9194C>T MANE Select | ENSP00000356379.4:p.Ala3065Val | |
| ENST00000680265.1:c.9416C>T | ENSP00000505384.1:p.Ala3139Val | |
| ENST00000680710.1:c.9194C>T | ENSP00000506676.1:p.Ala3065Val | |
| ENST00000294732.11:c.4439C>T | ENSP00000294732.7:p.Ala1480Val | |
| ENST00000367408.5:c.2189C>T | ENSP00000356378.1:p.Ala730Val | |
| ENST00000367409.8:c.9194C>T | ENSP00000356379.4:p.Ala3065Val | |
| ENST00000612785.1:c.3152C>T | ENSP00000479244.1:p.Ala1051Val | |
| NM_001206846.1:c.4439C>T | NP_001193775.1:p.Ala1480Val | |
| NM_018136.4:c.9194C>T | NP_060606.3:p.Ala3065Val | |
| NM_018136.5:c.9194C>T MANE Select | NP_060606.3:p.Ala3065Val | |
| NM_001206846.2:c.4439C>T | NP_001193775.1:p.Ala1480Val |