HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186166816G>A , CM000663.2:g.186166816G>A | GRCh38 |
NC_000001.10:g.186135948G>A , CM000663.1:g.186135948G>A | GRCh37 |
NC_000001.9:g.184402571G>A | NCBI36 |
NG_011841.1:g.437266G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271588.9:c.15448G>A MANE Select | ENSP00000271588.4:p.Glu5150Lys | |
ENST00000271588.8:c.15448G>A | ENSP00000271588.4:p.Glu5150Lys | |
ENST00000475585.1:n.163-4521G>A | ||
NM_031935.2:c.15448G>A | NP_114141.2:p.Glu5150Lys | |
XM_011510037.1:c.15163G>A | XP_011508339.1:p.Glu5055Lys | |
XM_011510038.1:c.15448G>A | XP_011508340.1:p.Glu5150Lys | |
XM_011510038.3:c.15448G>A | XP_011508340.1:p.Glu5150Lys | |
XM_017002437.1:c.13471G>A | XP_016857926.1:p.Glu4491Lys | |
NM_031935.3:c.15448G>A MANE Select | NP_114141.2:p.Glu5150Lys |