Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.228158963C= , CM000663.2:g.228158963C= | GRCh38 |
| NC_000001.10:g.228346664C= , CM000663.1:g.228346664C= | GRCh37 |
| NC_000001.9:g.226413287C= | NCBI36 |
| NG_011838.1:g.14112C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020435.4:c.1205C= MANE Select | NP_065168.2:p.Thr402= |
| ENST00000366714.3:c.1205C= MANE Select | ENSP00000355675.2:p.Thr402= |
| NM_020435.3:c.1205C= | NP_065168.2:p.Thr402= |
| ENST00000366714.2:c.1205C= | ENSP00000355675.2:p.Thr402= |