HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367847C>A , CM000677.2:g.73367847C>A | GRCh38 |
NC_000015.9:g.73660188C>A , CM000677.1:g.73660188C>A | GRCh37 |
NC_000015.8:g.71447241C>A | NCBI36 |
NG_009063.1:g.6418G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.424G>T MANE Select | ENSP00000261917.3:p.Asp142Tyr | |
ENST00000261917.3:c.424G>T | ENSP00000261917.3:p.Asp142Tyr | |
NM_005477.2:c.424G>T | NP_005468.1:p.Asp142Tyr | |
NM_005477.3:c.424G>T MANE Select | NP_005468.1:p.Asp142Tyr |