Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55114289C>A , CM000666.2:g.55114289C>A | GRCh38 |
| NC_000004.11:g.55980456C>A , CM000666.1:g.55980456C>A | GRCh37 |
| NC_000004.10:g.55675213C>A | NCBI36 |
| NG_012004.1:g.16307G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002253.4:c.659-24G>T MANE Select | NP_002244.1:n.659-24G>T |
| ENST00000263923.5:c.659-24G>T MANE Select | ENSP00000263923.4:n.659-24G>T |
| NM_002253.2:c.659-24G>T | NP_002244.1:n.659-24G>T |
| NM_002253.3:c.659-24G>T | NP_002244.1:n.659-24G>T |
| ENST00000263923.4:c.659-24G>T | ENSP00000263923.4:n.659-24G>T |
| ENST00000512566.1:n.659-24G>T | |
| ENST00000647068.1:n.672-24G>T |