Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117799891G>A , CM000670.2:g.117799891G>A | GRCh38 |
| NC_000008.10:g.118812130G>A , CM000670.1:g.118812130G>A | GRCh37 |
| NC_000008.9:g.118881311G>A | NCBI36 |
| NG_007455.2:g.316929C>T , LRG_493:g.316929C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.2062C>T MANE Select | NP_000118.2:p.Arg688Trp |
| ENST00000378204.7:c.2062C>T MANE Select | ENSP00000367446.3:p.Arg688Trp |
| NM_000127.2:c.2062C>T , LRG_493t1:c.2062C>T | NP_000118.2:p.Arg688Trp |
| ENST00000378204.6:c.2062C>T | ENSP00000367446.2:p.Arg688Trp |
| ENST00000437196.1:c.*953C>T | ENSP00000407299.1:n.*953C>T |
| ENST00000684189.1:n.1529C>T | |
| ENST00000684443.1:n.2188C>T |