dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.175441837T>A , CM000667.2:g.175441837T>A | GRCh38 |
| NC_000005.9:g.174868840T>A , CM000667.1:g.174868840T>A | GRCh37 |
| NC_000005.8:g.174801446T>A | NCBI36 |
| NG_011802.1:g.7324A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393752.3:c.1263A>T MANE Select | ENSP00000377353.1:p.Ser421= | |
| ENST00000393752.2:c.1263A>T | ENSP00000377353.1:p.Ser421= | |
| NM_000794.3:c.1263A>T | NP_000785.1:p.Ser421= | |
| NM_000794.4:c.1263A>T | NP_000785.1:p.Ser421= | |
| NM_000794.5:c.1263A>T MANE Select | NP_000785.1:p.Ser421= |