HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367804C>T , CM000677.2:g.73367804C>T | GRCh38 |
NC_000015.9:g.73660145C>T , CM000677.1:g.73660145C>T | GRCh37 |
NC_000015.8:g.71447198C>T | NCBI36 |
NG_009063.1:g.6461G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.467G>A MANE Select | ENSP00000261917.3:p.Gly156Asp | |
ENST00000261917.3:c.467G>A | ENSP00000261917.3:p.Gly156Asp | |
NM_005477.2:c.467G>A | NP_005468.1:p.Gly156Asp | |
NM_005477.3:c.467G>A MANE Select | NP_005468.1:p.Gly156Asp |