Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129532430G= , CM000665.2:g.129532430G= | GRCh38 |
| NC_000003.11:g.129251273G= , CM000665.1:g.129251273G= | GRCh37 |
| NC_000003.10:g.130733963G= | NCBI36 |
| NG_009115.1:g.8792G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.696+14G= MANE Select | ENSP00000296271.3:n.696+14G= | |
| ENST00000296271.3:c.696+14G= | ENSP00000296271.3:n.696+14G= | |
| NM_000539.3:c.696+14G= MANE Select | NP_000530.1:n.696+14G= |