HGVS | Genome Assembly |
---|---|
NC_000021.9:g.17796838G>T , CM000683.2:g.17796838G>T | GRCh38 |
NC_000021.8:g.19169155G>T , CM000683.1:g.19169155G>T | GRCh37 |
NC_000021.7:g.18091026G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284881.9:c.408C>A MANE Select | ENSP00000284881.4:p.Asp136Glu | |
ENST00000284881.8:c.408C>A | ENSP00000284881.4:p.Asp136Glu | |
ENST00000400558.7:c.408C>A | ENSP00000383403.3:p.Asp136Glu | |
ENST00000400559.7:c.408C>A | ENSP00000383404.3:p.Asp136Glu | |
ENST00000405964.2:c.408C>A | ENSP00000385566.2:p.Asp136Glu | |
ENST00000493464.1:n.629C>A | ||
NM_001100420.1:c.408C>A | NP_001093890.1:p.Asp136Glu | |
NM_001100421.1:c.408C>A | NP_001093891.1:p.Asp136Glu | |
NM_017447.3:c.408C>A | NP_059143.3:p.Asp136Glu | |
NM_001100420.2:c.408C>A MANE Select | NP_001093890.1:p.Asp136Glu | |
NM_001100421.2:c.408C>A | NP_001093891.1:p.Asp136Glu | |
NM_017447.4:c.408C>A | NP_059143.3:p.Asp136Glu |