Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134490192T>A , CM000685.2:g.134490192T>A | GRCh38 |
| NC_000023.10:g.133624222T>A , CM000685.1:g.133624222T>A | GRCh37 |
| NC_000023.9:g.133451888T>A | NCBI36 |
| NG_012329.1:g.35048T>A | |
| NG_012329.2:g.35048T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000298556.8:c.389T>A MANE Select | ENSP00000298556.7:p.Val130Asp | |
| ENST00000298556.7:c.389T>A | ENSP00000298556.7:p.Val130Asp | |
| ENST00000462974.5:n.547T>A | ||
| ENST00000475720.1:n.347T>A | ||
| NM_000194.2:c.389T>A | NP_000185.1:p.Val130Asp | |
| XM_011531328.1:c.407T>A | XP_011529630.1:p.Val136Asp | |
| NM_000194.3:c.389T>A MANE Select | NP_000185.1:p.Val130Asp |