Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31271270G= , CM000668.2:g.31271270G= | GRCh38 |
| NC_000006.11:g.31239047G= , CM000668.1:g.31239047G= | GRCh37 |
| NC_000006.10:g.31347026G= | NCBI36 |
| NG_029422.2:g.5862C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.422C= MANE Select | ENSP00000365402.5:p.Ala141= | |
| ENST00000376228.9:c.422C= | ENSP00000365402.5:p.Ala141= | |
| ENST00000376237.8:c.*9C= | ENSP00000365412.4:n.*9C= | |
| ENST00000383329.7:c.422C= | ENSP00000372819.3:p.Ala141= | |
| ENST00000415537.1:c.420C= | ||
| ENST00000484378.1:n.691C= | ||
| ENST00000487245.5:n.781C= | ||
| ENST00000495835.1:n.611C= | ||
| NM_002117.5:c.422C= | NP_002108.4:p.Ala141= | |
| NM_002117.6:c.422C= MANE Select | NP_002108.4:p.Ala141= |