Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270834G= , CM000668.2:g.31270834G= | GRCh38 |
| NC_000006.11:g.31238611G= , CM000668.1:g.31238611G= | GRCh37 |
| NC_000006.10:g.31346590G= | NCBI36 |
| NG_029422.2:g.6298C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.619+239C= MANE Select | ENSP00000365402.5:n.619+239C= | |
| ENST00000376228.9:c.619+239C= | ENSP00000365402.5:n.619+239C= | |
| ENST00000376237.8:c.*206+239C= | ENSP00000365412.4:n.*206+239C= | |
| ENST00000383329.7:c.619+239C= | ENSP00000372819.3:n.619+239C= | |
| ENST00000415537.1:c.617+239C= | ||
| ENST00000487245.5:n.978+239C= | ||
| ENST00000495835.1:n.808+239C= | ||
| NM_002117.5:c.619+239C= | NP_002108.4:n.619+239C= | |
| NM_002117.6:c.619+239C= MANE Select | NP_002108.4:n.619+239C= |