Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73329719C= , CM000677.2:g.73329719C= | GRCh38 |
| NC_000015.9:g.73622060C= , CM000677.1:g.73622060C= | GRCh37 |
| NC_000015.8:g.71409113C= | NCBI36 |
| NG_009063.1:g.44546G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005477.3:c.1444G= MANE Select | NP_005468.1:p.Gly482= |
| ENST00000261917.4:c.1444G= MANE Select | ENSP00000261917.3:p.Gly482= |
| NM_005477.2:c.1444G= | NP_005468.1:p.Gly482= |
| ENST00000261917.3:c.1444G= | ENSP00000261917.3:p.Gly482= |
| XM_011521148.1:c.226G= | XP_011519450.1:p.Gly76= |
| XM_011521148.2:c.226G= | XP_011519450.1:p.Gly76= |