Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.172665636A>T , CM000663.2:g.172665636A>T | GRCh38 |
| NC_000001.10:g.172634776A>T , CM000663.1:g.172634776A>T | GRCh37 |
| NC_000001.9:g.170901399A>T | NCBI36 |
| NG_007269.1:g.11592A>T , LRG_58:g.11592A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000639.3:c.466A>T MANE Select | NP_000630.1:p.Arg156Trp |
| ENST00000367721.3:c.466A>T MANE Select | ENSP00000356694.2:p.Arg156Trp |
| NM_000639.2:c.466A>T | NP_000630.1:p.Arg156Trp |
| NM_001302746.1:c.*36A>T | NP_001289675.1:n.*36A>T |
| NM_001302746.2:c.*36A>T | NP_001289675.1:n.*36A>T |
| ENST00000340030.4:c.*36A>T | ENSP00000344739.3:n.*36A>T |
| ENST00000367721.2:c.466A>T | ENSP00000356694.2:p.Arg156Trp |