Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981649G>A , CM000674.2:g.48981649G>A | GRCh38 |
| NC_000012.11:g.49375432G>A , CM000674.1:g.49375432G>A | GRCh37 |
| NC_000012.10:g.47661699G>A | NCBI36 |
| NG_033141.1:g.8197G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005430.4:c.*9G>A MANE Select | NP_005421.1:n.*9G>A |
| ENST00000293549.4:c.*9G>A MANE Select | ENSP00000293549.3:n.*9G>A |
| NM_005430.3:c.*9G>A | NP_005421.1:n.*9G>A |
| ENST00000293549.3:c.*9G>A | ENSP00000293549.3:n.*9G>A |