Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112226397G>A , CM000673.2:g.112226397G>A | GRCh38 |
| NC_000011.9:g.112097120G>A , CM000673.1:g.112097120G>A | GRCh37 |
| NC_000011.8:g.111602330G>A | NCBI36 |
| NG_008743.1:g.5033G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000280362.7:c.-47G>A | ENSP00000280362.3:n.-47G>A | |
| ENST00000525645.1:n.29G>A | ||
| ENST00000528679.5:c.-47G>A | ENSP00000435895.1:n.-47G>A | |
| ENST00000531673.5:c.-47G>A | ENSP00000433469.1:n.-47G>A | |
| NM_000317.2:c.-47G>A | NP_000308.1:n.-47G>A |