Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133365857A>C , CM000672.2:g.133365857A>C | GRCh38 |
| NC_000010.10:g.135179361A>C , CM000672.1:g.135179361A>C | GRCh37 |
| NC_000010.9:g.135029351A>C | NCBI36 |
| NG_042077.1:g.12548T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368547.4:c.739+119T>G MANE Select | ENSP00000357535.3:n.739+119T>G | |
| ENST00000368547.3:c.739+119T>G | ENSP00000357535.3:n.739+119T>G | |
| NM_004092.3:c.739+119T>G | NP_004083.3:n.739+119T>G | |
| XR_002956965.1:n.1595+119T>G | ||
| NM_004092.4:c.739+119T>G MANE Select | NP_004083.3:n.739+119T>G |