Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184060298C= , CM000665.2:g.184060298C= | GRCh38 |
| NC_000003.11:g.183778086C= , CM000665.1:g.183778086C= | GRCh37 |
| NC_000003.10:g.185260780C= | NCBI36 |
| NG_012749.1:g.12252C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318351.2:c.1290C= MANE Select | ENSP00000322617.1:p.Tyr430= | |
| ENST00000318351.1:c.1290C= | ENSP00000322617.1:p.Tyr430= | |
| NM_130770.2:c.1290C= | NP_570126.2:p.Tyr430= | |
| NM_130770.3:c.1290C= MANE Select | NP_570126.2:p.Tyr430= |