Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6718117G>A , CM000681.2:g.6718117G>A | GRCh38 |
| NC_000019.9:g.6718128G>A , CM000681.1:g.6718128G>A | GRCh37 |
| NC_000019.8:g.6669128G>A | NCBI36 |
| NG_009557.1:g.7535C>T , LRG_27:g.7535C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000594936.2:n.542C>T | ||
| ENST00000695652.1:c.358C>T | ENSP00000512083.1:p.Arg120Trp | |
| ENST00000695693.1:c.481C>T | ENSP00000512104.1:p.Arg161Trp | |
| ENST00000245907.11:c.481C>T MANE Select | ENSP00000245907.4:p.Arg161Trp | |
| ENST00000245907.10:c.481C>T | ENSP00000245907.4:p.Arg161Trp | |
| ENST00000594936.1:n.542C>T | ||
| NM_000064.3:c.481C>T | NP_000055.2:p.Arg161Trp | |
| NM_000064.4:c.481C>T MANE Select | NP_000055.2:p.Arg161Trp |