Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924271C= , CM000675.2:g.27924271C= | GRCh38 |
| NC_000013.10:g.28498408C= , CM000675.1:g.28498408C= | GRCh37 |
| NC_000013.9:g.27396408C= | NCBI36 |
| NG_008183.1:g.9241C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.422C= MANE Select | ENSP00000370421.4:p.Ala141= | |
| ENST00000381033.4:c.422C= | ENSP00000370421.4:p.Ala141= | |
| NM_000209.3:c.422C= | NP_000200.1:p.Ala141= | |
| XR_941578.1:n.3549C= | ||
| XR_941579.1:n.2148C= | ||
| XR_941580.1:n.1064C= | ||
| XR_941578.2:n.3561C= | ||
| XR_941580.2:n.1076C= | ||
| NM_000209.4:c.422C= MANE Select | NP_000200.1:p.Ala141= |