Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81536998G>A , CM000665.2:g.81536998G>A | GRCh38 |
| NC_000003.11:g.81586149G>A , CM000665.1:g.81586149G>A | GRCh37 |
| NC_000003.10:g.81668839G>A | NCBI36 |
| NG_011810.1:g.229803C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.1716C>T MANE Select | ENSP00000410833.2:p.Asp572= | |
| ENST00000429644.6:c.1716C>T | ENSP00000410833.2:p.Asp572= | |
| ENST00000484687.1:n.117C>T | ||
| ENST00000489715.1:c.1593C>T | ENSP00000419638.1:p.Asp531= | |
| NM_000158.3:c.1716C>T | NP_000149.3:p.Asp572= | |
| NM_000158.4:c.1716C>T MANE Select | NP_000149.4:p.Asp572= |