Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134493508G>T , CM000685.2:g.134493508G>T | GRCh38 |
| NC_000023.10:g.133627538G>T , CM000685.1:g.133627538G>T | GRCh37 |
| NC_000023.9:g.133455204G>T | NCBI36 |
| NG_012329.1:g.38364G>T | |
| NG_012329.2:g.38364G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000194.3:c.403G>T MANE Select | NP_000185.1:p.Asp135Tyr |
| ENST00000298556.8:c.403G>T MANE Select | ENSP00000298556.7:p.Asp135Tyr |
| NM_000194.2:c.403G>T | NP_000185.1:p.Asp135Tyr |
| ENST00000298556.7:c.403G>T | ENSP00000298556.7:p.Asp135Tyr |
| ENST00000462974.5:n.561G>T | |
| ENST00000475720.1:n.361G>T | |
| XM_011531328.1:c.421G>T | XP_011529630.1:p.Asp141Tyr |