Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184059868C= , CM000665.2:g.184059868C= | GRCh38 |
| NC_000003.11:g.183777656C= , CM000665.1:g.183777656C= | GRCh37 |
| NC_000003.10:g.185260350C= | NCBI36 |
| NG_012749.1:g.11822C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318351.2:c.966C= MANE Select | ENSP00000322617.1:p.Ser322= | |
| ENST00000318351.1:c.966C= | ENSP00000322617.1:p.Ser322= | |
| NM_130770.2:c.966C= | NP_570126.2:p.Ser322= | |
| NM_130770.3:c.966C= MANE Select | NP_570126.2:p.Ser322= |