Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57194266A>G , CM000674.2:g.57194266A>G | GRCh38 |
| NC_000012.11:g.57588049A>G , CM000674.1:g.57588049A>G | GRCh37 |
| NC_000012.10:g.55874316A>G | NCBI36 |
| NG_016444.1:g.70768A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002332.3:c.7919-88A>G MANE Select | NP_002323.2:n.7919-88A>G |
| ENST00000243077.8:c.7919-88A>G MANE Select | ENSP00000243077.3:n.7919-88A>G |
| NM_002332.2:c.7919-88A>G | NP_002323.2:n.7919-88A>G |
| ENST00000243077.7:c.7919-88A>G | ENSP00000243077.3:n.7919-88A>G |
| XM_017019303.1:c.7970-88A>G | XP_016874792.1:n.7970-88A>G |