Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45777136A>G , CM000679.2:g.45777136A>G | GRCh38 |
| NC_000017.10:g.43854502A>G , CM000679.1:g.43854502A>G | GRCh37 |
| NC_000017.9:g.41210268A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001256299.2:c.-492-29874A>G | NP_001243228.1:n.-492-29874A>G |
| NM_001256299.3:c.-492-29874A>G | NP_001243228.1:n.-492-29874A>G |
| NM_001303016.1:c.-184-29874A>G | NP_001289945.1:n.-184-29874A>G |
| ENST00000587305.1:n.448-29874A>G | |
| ENST00000634540.1:c.-492-29874A>G | ENSP00000488912.1:n.-492-29874A>G |