Linked Data
dbSNP Id:
rs746970098
ExAC:
3:43740785 G / A
gnomAD v2:
3-43740785-G-A
gnomAD v4:
3-43699293-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.43699293G>A , CM000665.2:g.43699293G>A | GRCh38 |
| NC_000003.11:g.43740785G>A , CM000665.1:g.43740785G>A | GRCh37 |
| NC_000003.10:g.43715789G>A | NCBI36 |
| NG_007090.3:g.13411G>A | |
| NG_007090.5:g.13424G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000013894.3:c.65G>A | ENSP00000013894.2:p.Gly22Asp | |
| ENST00000454293.2:c.-59G>A | ENSP00000412014.2:n.-59G>A | |
| ENST00000458276.7:c.65G>A | ENSP00000390849.3:p.Gly22Asp | |
| ENST00000642351.1:c.-59G>A | ENSP00000494478.1:n.-59G>A | |
| ENST00000643140.1:c.65G>A | ENSP00000495588.1:p.Gly22Asp | |
| ENST00000643477.1:c.65G>A | ENSP00000496220.1:p.Gly22Asp | |
| ENST00000643500.1:c.65G>A | ENSP00000494735.1:p.Gly22Asp | |
| ENST00000643520.1:n.113G>A | ||
| ENST00000644371.2:c.65G>A MANE Select | ENSP00000495778.1:p.Gly22Asp | |
| ENST00000646378.1:c.*115G>A | ENSP00000495826.1:n.*115G>A | |
| ENST00000646799.1:c.65G>A | ENSP00000494829.1:p.Gly22Asp | |
| ENST00000649763.1:c.65G>A | ENSP00000497701.1:p.Gly22Asp | |
| ENST00000013894.2:c.65G>A | ENSP00000013894.2:p.Gly22Asp | |
| ENST00000454293.1:c.-59G>A | ENSP00000412014.1:n.-59G>A | |
| ENST00000456453.5:c.-59G>A | ENSP00000391582.1:n.-59G>A | |
| ENST00000458276.6:c.65G>A | ENSP00000390849.2:p.Gly22Asp | |
| ENST00000486764.1:n.166G>A | ||
| NM_016006.4:c.65G>A | NP_057090.2:p.Gly22Asp | |
| XM_011533779.1:c.-59G>A | XP_011532081.1:n.-59G>A | |
| XM_011533780.1:c.65G>A | XP_011532082.1:p.Gly22Asp | |
| XR_940447.1:n.122G>A | ||
| NM_001355186.1:c.65G>A | NP_001342115.1:p.Gly22Asp | |
| NM_001365649.1:c.-59G>A | NP_001352578.1:n.-59G>A | |
| NM_001365650.1:c.65G>A | NP_001352579.1:p.Gly22Asp | |
| NM_016006.5:c.65G>A | NP_057090.2:p.Gly22Asp | |
| NR_158560.1:n.188G>A | ||
| NM_001355186.2:c.65G>A | NP_001342115.1:p.Gly22Asp | |
| NM_016006.6:c.65G>A MANE Select | NP_057090.2:p.Gly22Asp |