Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.68249832C= , CM000674.2:g.68249832C= | GRCh38 |
| NC_000012.11:g.68643612C= , CM000674.1:g.68643612C= | GRCh37 |
| NC_000012.10:g.66929879C= | NCBI36 |
| NG_060763.1:g.8773G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328087.6:c.463-956G= | ENSP00000329384.4:n.463-956G= | |
| ENST00000538666.6:c.463-956G= MANE Select | ENSP00000442424.1:n.463-956G= | |
| ENST00000328087.5:c.463-956G= | ENSP00000329384.4:n.463-956G= | |
| ENST00000538666.5:c.463-956G= | ENSP00000442424.1:n.463-956G= | |
| NM_020525.4:c.463-956G= | NP_065386.1:n.463-956G= | |
| XR_945055.1:n.265-14826C= | ||
| NM_020525.5:c.463-956G= MANE Select | NP_065386.1:n.463-956G= | |
| XR_002957418.1:n.281-14826C= |