Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.5693289G>T , CM000664.2:g.5693289G>T | GRCh38 |
| NC_000002.11:g.5833421G>T , CM000664.1:g.5833421G>T | GRCh37 |
| NC_000002.10:g.5750872G>T | NCBI36 |
| NG_050751.1:g.5623G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003108.4:c.568G>T MANE Select | NP_003099.1:p.Asp190Tyr |
| ENST00000322002.5:c.568G>T MANE Select | ENSP00000322568.3:p.Asp190Tyr |
| NM_003108.3:c.568G>T | NP_003099.1:p.Asp190Tyr |
| ENST00000322002.4:c.568G>T | ENSP00000322568.3:p.Asp190Tyr |