Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38408964G= , CM000685.2:g.38408964G= | GRCh38 |
| NC_000023.10:g.38268217G= , CM000685.1:g.38268217G= | GRCh37 |
| NC_000023.9:g.38153161G= | NCBI36 |
| NG_008471.1:g.61482G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.806G= MANE Select | ENSP00000039007.4:p.Gly269= | |
| ENST00000643344.1:c.*556G= | ENSP00000496606.1:n.*556G= | |
| ENST00000039007.4:c.806G= | ENSP00000039007.4:p.Gly269= | |
| ENST00000465127.1:c.172-257157G= | ENSP00000417050.1:n.172-257157G= | |
| NM_000531.5:c.806G= | NP_000522.3:p.Gly269= | |
| XM_017029556.1:c.806G= | XP_016885045.1:p.Gly269= | |
| NM_000531.6:c.806G= MANE Select | NP_000522.3:p.Gly269= |