Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38421032G= , CM000685.2:g.38421032G= | GRCh38 |
| NC_000023.10:g.38280285G= , CM000685.1:g.38280285G= | GRCh37 |
| NC_000023.9:g.38165229G= | NCBI36 |
| NG_008471.1:g.73550G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.1015G= MANE Select | NP_000522.3:p.Val339= |
| ENST00000039007.5:c.1015G= MANE Select | ENSP00000039007.4:p.Val339= |
| NM_000531.5:c.1015G= | NP_000522.3:p.Val339= |
| ENST00000039007.4:c.1015G= | ENSP00000039007.4:p.Val339= |
| ENST00000465127.1:c.172-245089G= | ENSP00000417050.1:n.172-245089G= |
| ENST00000643344.1:c.*765G= | ENSP00000496606.1:n.*765G= |