HGVS | Genome Assembly |
---|---|
NC_000019.10:g.3770677G>A , CM000681.2:g.3770677G>A | GRCh38 |
NC_000019.9:g.3770675G>A , CM000681.1:g.3770675G>A | GRCh37 |
NC_000019.8:g.3721675G>A | NCBI36 |
NG_011565.1:g.6545C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555633.3:c.499C>T MANE Select | ENSP00000450456.3:p.Arg167Trp | |
ENST00000555633.2:c.499C>T | ENSP00000450456.2:p.Arg167Trp | |
ENST00000555978.5:c.499C>T | ENSP00000450687.2:p.Arg167Trp | |
NM_032753.3:c.499C>T | NP_116142.1:p.Arg167Trp | |
XM_005259662.1:c.637C>T | XP_005259719.1:p.Arg213Trp | |
NM_001319074.1:c.637C>T | NP_001306003.1:p.Arg213Trp | |
NM_001319074.4:c.499C>T MANE Select | NP_001306003.2:p.Arg167Trp | |
NM_032753.4:c.499C>T | NP_116142.1:p.Arg167Trp |