Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68829738G>A , CM000685.2:g.68829738G>A | GRCh38 |
| NC_000023.10:g.68049581G>A , CM000685.1:g.68049581G>A | GRCh37 |
| NC_000023.9:g.67966306G>A | NCBI36 |
| NG_008887.1:g.5742G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.-39G>A MANE Select | ENSP00000204961.4:n.-39G>A | |
| ENST00000204961.4:c.-39G>A | ENSP00000204961.4:n.-39G>A | |
| NM_004429.4:c.-39G>A | NP_004420.1:n.-39G>A | |
| NM_004429.5:c.-39G>A MANE Select | NP_004420.1:n.-39G>A |