HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978158G>A , CM000667.2:g.149978158G>A | GRCh38 |
NC_000005.9:g.149357721G>A , CM000667.1:g.149357721G>A | GRCh37 |
NC_000005.8:g.149337914G>A | NCBI36 |
NG_007147.2:g.19276G>A , LRG_684:g.19276G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.738G>A | ||
ENST00000286298.5:c.506G>A MANE Select | ENSP00000286298.4:p.Cys169Tyr | |
ENST00000286298.4:c.506G>A | ENSP00000286298.4:p.Cys169Tyr | |
ENST00000503336.1:c.179G>A | ENSP00000426053.1:p.Cys60Tyr | |
NM_000112.3:c.506G>A , LRG_684t1:c.506G>A | NP_000103.2:p.Cys169Tyr | |
XM_017009191.2:c.506G>A | XP_016864680.1:p.Cys169Tyr | |
NM_000112.4:c.506G>A MANE Select | NP_000103.2:p.Cys169Tyr |