Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38352558A>G , CM000685.2:g.38352558A>G | GRCh38 |
| NC_000023.10:g.38211811A>G , CM000685.1:g.38211811A>G | GRCh37 |
| NC_000023.9:g.38096755A>G | NCBI36 |
| NG_008471.1:g.5076A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.4:c.-139A>G | ENSP00000039007.4:n.-139A>G | |
| ENST00000465127.1:c.172-313563A>G | ENSP00000417050.1:n.172-313563A>G | |
| NM_000531.5:c.-139A>G | NP_000522.3:n.-139A>G | |
| XM_017029556.1:c.-139A>G | XP_016885045.1:n.-139A>G |