Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.28863085C= , CM000663.2:g.28863085C= | GRCh38 |
| NC_000001.10:g.29189597C= , CM000663.1:g.29189597C= | GRCh37 |
| NC_000001.9:g.29062184C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000911.4:c.921C= MANE Select | NP_000902.3:p.Gly307= |
| ENST00000234961.7:c.921C= MANE Select | ENSP00000234961.2:p.Gly307= |
| NM_000911.3:c.921C= | NP_000902.3:p.Gly307= |
| ENST00000234961.6:c.921C= | ENSP00000234961.2:p.Gly307= |
| ENST00000621425.1:c.777C= | ENSP00000477970.1:p.Gly259= |