Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.121339035C= , CM000669.2:g.121339035C= | GRCh38 |
| NC_000007.13:g.120979089C= , CM000669.1:g.120979089C= | GRCh37 |
| NC_000007.12:g.120766325C= | NCBI36 |
| NG_029242.1:g.18669C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_057168.2:c.788C= MANE Select | NP_476509.1:p.Thr263= |
| ENST00000222462.3:c.788C= MANE Select | ENSP00000222462.2:p.Thr263= |
| NM_016087.2:c.758C= | NP_057171.2:p.Thr253= |
| NM_057168.1:c.788C= | NP_476509.1:p.Thr263= |
| ENST00000222462.2:c.788C= | ENSP00000222462.2:p.Thr263= |
| ENST00000361301.6:c.758C= | ENSP00000355065.2:p.Thr253= |