Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38411938T>G , CM000685.2:g.38411938T>G | GRCh38 |
| NC_000023.10:g.38271191T>G , CM000685.1:g.38271191T>G | GRCh37 |
| NC_000023.9:g.38156135T>G | NCBI36 |
| NG_008471.1:g.64456T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000039007.5:c.944T>G MANE Select | ENSP00000039007.4:p.Val315Gly | |
| ENST00000643344.1:c.*694T>G | ENSP00000496606.1:n.*694T>G | |
| ENST00000039007.4:c.944T>G | ENSP00000039007.4:p.Val315Gly | |
| ENST00000465127.1:c.172-254183T>G | ENSP00000417050.1:n.172-254183T>G | |
| NM_000531.5:c.944T>G | NP_000522.3:p.Val315Gly | |
| NM_000531.6:c.944T>G MANE Select | NP_000522.3:p.Val315Gly |