Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520375A>G , CM000674.2:g.52520375A>G | GRCh38 |
| NC_000012.11:g.52914159A>G , CM000674.1:g.52914159A>G | GRCh37 |
| NC_000012.10:g.51200426A>G | NCBI36 |
| NG_008297.1:g.5085T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.-79T>C MANE Select | ENSP00000252242.4:n.-79T>C | |
| ENST00000252242.8:c.-79T>C | ENSP00000252242.4:n.-79T>C | |
| ENST00000546577.1:c.-13+22T>C | ENSP00000449651.1:n.-13+22T>C | |
| ENST00000551275.1:c.-79T>C | ENSP00000448041.1:n.-79T>C | |
| ENST00000552629.5:n.20T>C | ||
| NM_000424.3:c.-79T>C | NP_000415.2:n.-79T>C | |
| NM_000424.4:c.-79T>C MANE Select | NP_000415.2:n.-79T>C |