Linked Data
dbSNP Id:
rs1012286392
gnomAD v2:
10-82033356-C-T
gnomAD v3:
10-80273600-C-T
gnomAD v4:
10-80273600-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80273600C>T , CM000672.2:g.80273600C>T | GRCh38 |
| NC_000010.10:g.82033356C>T , CM000672.1:g.82033356C>T | GRCh37 |
| NC_000010.9:g.82023336C>T | NCBI36 |
| NG_008083.1:g.21079G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.*181G>A MANE Select | ENSP00000361287.3:n.*181G>A | |
| ENST00000372213.7:c.*181G>A | ENSP00000361287.3:n.*181G>A | |
| ENST00000480845.1:n.601G>A | ||
| ENST00000485270.5:n.881G>A | ||
| NM_000429.2:c.*181G>A | NP_000420.1:n.*181G>A | |
| XM_005269842.3:c.*181G>A | XP_005269899.1:n.*181G>A | |
| XM_005269843.3:c.*181G>A | XP_005269900.1:n.*181G>A | |
| NM_000429.3:c.*181G>A MANE Select | NP_000420.1:n.*181G>A |