Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38401373G= , CM000685.2:g.38401373G= | GRCh38 |
| NC_000023.10:g.38260626G= , CM000685.1:g.38260626G= | GRCh37 |
| NC_000023.9:g.38145570G= | NCBI36 |
| NG_008471.1:g.53891G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.485G= MANE Select | ENSP00000039007.4:p.Gly162= | |
| ENST00000643344.1:c.*235G= | ENSP00000496606.1:n.*235G= | |
| ENST00000039007.4:c.485G= | ENSP00000039007.4:p.Gly162= | |
| ENST00000465127.1:c.172-264748G= | ENSP00000417050.1:n.172-264748G= | |
| ENST00000488812.1:n.522G= | ||
| NM_000531.5:c.485G= | NP_000522.3:p.Gly162= | |
| XM_017029556.1:c.485G= | XP_016885045.1:p.Gly162= | |
| NM_000531.6:c.485G= MANE Select | NP_000522.3:p.Gly162= |