HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992932C>T , CM000667.2:g.177992932C>T | GRCh38 |
NC_000005.9:g.177419933C>T , CM000667.1:g.177419933C>T | GRCh37 |
NC_000005.8:g.177352539C>T | NCBI36 |
NG_015889.1:g.8311G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.458G>A MANE Select | ENSP00000311290.2:p.Cys153Tyr | |
NM_006261.4:c.458G>A | NP_006252.3:p.Cys153Tyr | |
NM_006261.5:c.458G>A MANE Select | NP_006252.4:p.Cys153Tyr |