Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31541226G= , CM000680.2:g.31541226G= | GRCh38 |
| NC_000018.9:g.29121189G= , CM000680.1:g.29121189G= | GRCh37 |
| NC_000018.8:g.27375187G= | NCBI36 |
| NG_007072.3:g.47985G= , LRG_397:g.47985G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.1913G= MANE Select | ENSP00000261590.8:p.Gly638= | |
| ENST00000261590.12:c.1913G= | ENSP00000261590.8:p.Gly638= | |
| NM_001943.3:c.1913G= , LRG_397t1:c.1913G= | NP_001934.2:p.Gly638= | |
| NM_001943.4:c.1913G= | NP_001934.2:p.Gly638= | |
| XM_024451095.1:c.1379G= | XP_024306863.1:p.Gly460= | |
| NM_001943.5:c.1913G= MANE Select | NP_001934.2:p.Gly638= |