Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38146158A>T , CM000670.2:g.38146158A>T | GRCh38 |
| NC_000008.10:g.38003676A>T , CM000670.1:g.38003676A>T | GRCh37 |
| NC_000008.9:g.38122833A>T | NCBI36 |
| NG_011827.1:g.9925T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000349.3:c.466-11T>A MANE Select | NP_000340.2:n.466-11T>A |
| ENST00000276449.9:c.466-11T>A MANE Select | ENSP00000276449.3:n.466-11T>A |
| NM_000349.2:c.466-11T>A | NP_000340.2:n.466-11T>A |
| ENST00000276449.8:c.466-11T>A | ENSP00000276449.3:n.466-11T>A |
| ENST00000520114.1:n.953-11T>A | |
| ENST00000522050.1:c.402-11T>A | |
| XM_006716392.1:c.466-11T>A | XP_006716455.1:n.466-11T>A |