Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144222G= , CM000670.2:g.38144222G= | GRCh38 |
| NC_000008.10:g.38001740G= , CM000670.1:g.38001740G= | GRCh37 |
| NC_000008.9:g.38120897G= | NCBI36 |
| NG_011827.1:g.11861C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.*51C= MANE Select | ENSP00000276449.3:n.*51C= | |
| ENST00000276449.8:c.*51C= | ENSP00000276449.3:n.*51C= | |
| ENST00000520114.1:n.2878C= | ||
| NM_000349.2:c.*51C= | NP_000340.2:n.*51C= | |
| XM_006716392.1:c.815C= | XP_006716455.1:p.Ser272= | |
| NM_000349.3:c.*51C= MANE Select | NP_000340.2:n.*51C= |