Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115705191C>A , CM000663.2:g.115705191C>A | GRCh38 |
| NC_000001.10:g.116247812C>A , CM000663.1:g.116247812C>A | GRCh37 |
| NC_000001.9:g.116049335C>A | NCBI36 |
| NG_008802.1:g.68615G>T , LRG_404:g.68615G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001232.4:c.939+1G>T MANE Select | NP_001223.2:n.939+1G>T |
| ENST00000261448.6:c.939+1G>T MANE Select | ENSP00000261448.5:n.939+1G>T |
| NM_001232.3:c.939+1G>T , LRG_404t1:c.939+1G>T | NP_001223.2:n.939+1G>T |
| ENST00000261448.5:c.939+1G>T | ENSP00000261448.5:n.939+1G>T |
| ENST00000488931.2:c.*311+1G>T | ENSP00000518226.1:n.*311+1G>T |