Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31125743T>A , CM000668.2:g.31125743T>A | GRCh38 |
| NC_000006.11:g.31093520T>A , CM000668.1:g.31093520T>A | GRCh37 |
| NC_000006.10:g.31201499T>A | NCBI36 |
| NG_021348.1:g.15913T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259881.10:c.-161T>A MANE Select | ENSP00000259881.9:n.-161T>A | |
| ENST00000259881.9:c.-161T>A | ENSP00000259881.9:n.-161T>A | |
| ENST00000479581.5:n.61+10852T>A | ||
| ENST00000548049.1:n.184T>A | ||
| ENST00000550838.1:n.63T>A | ||
| ENST00000552747.1:n.53+10852T>A | ||
| NM_014068.2:c.-161T>A | NP_054787.2:n.-161T>A | |
| NM_014068.3:c.-161T>A MANE Select | NP_054787.2:n.-161T>A |