Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.159886494C= , CM000663.2:g.159886494C= | GRCh38 |
| NC_000001.10:g.159856284C= , CM000663.1:g.159856284C= | GRCh37 |
| NC_000001.9:g.158122908C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368099.9:c.767+17G= MANE Select | ENSP00000357079.4:n.767+17G= | |
| ENST00000368099.8:c.767+17G= | ENSP00000357079.4:n.767+17G= | |
| ENST00000426543.6:c.512+17G= | ENSP00000403044.2:n.512+17G= | |
| ENST00000476696.5:c.767+17G= | ENSP00000483972.1:n.767+17G= | |
| NM_012337.2:c.767+17G= | NP_036469.2:n.767+17G= | |
| NM_012337.3:c.767+17G= MANE Select | NP_036469.2:n.767+17G= |