Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240871433G>T , CM000664.2:g.240871433G>T | GRCh38 |
| NC_000002.11:g.241810850G>T , CM000664.1:g.241810850G>T | GRCh37 |
| NC_000002.10:g.241459523G>T | NCBI36 |
| NG_008005.1:g.7689G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000030.3:c.508G>T MANE Select | NP_000021.1:p.Gly170Trp |
| ENST00000307503.4:c.508G>T MANE Select | ENSP00000302620.3:p.Gly170Trp |
| NM_000030.2:c.508G>T | NP_000021.1:p.Gly170Trp |
| ENST00000307503.3:c.508G>T | ENSP00000302620.3:p.Gly170Trp |
| ENST00000472436.1:n.528G>T | |
| ENST00000476698.1:n.245G>T |