Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110164943C>A , CM000675.2:g.110164943C>A | GRCh38 |
| NC_000013.10:g.110817290C>A , CM000675.1:g.110817290C>A | GRCh37 |
| NC_000013.9:g.109615291C>A | NCBI36 |
| NG_011544.2:g.147207G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.4069G>T MANE Select | NP_001836.3:p.Gly1357Trp |
| ENST00000375820.10:c.4069G>T MANE Select | ENSP00000364979.4:p.Gly1357Trp |
| NM_001845.5:c.4069G>T | NP_001836.3:p.Gly1357Trp |
| ENST00000375820.8:c.4069G>T | ENSP00000364979.4:p.Gly1357Trp |
| ENST00000649720.1:n.237G>T | |
| ENST00000650424.1:c.225G>T | |
| XM_011521048.1:c.3877G>T | XP_011519350.1:p.Gly1293Trp |
| XM_011521048.2:c.3877G>T | XP_011519350.1:p.Gly1293Trp |