HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52519791C>A , CM000674.2:g.52519791C>A | GRCh38 |
NC_000012.11:g.52913575C>A , CM000674.1:g.52913575C>A | GRCh37 |
NC_000012.10:g.51199842C>A | NCBI36 |
NG_008297.1:g.5669G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252242.9:c.506G>T MANE Select | ENSP00000252242.4:p.Arg169Leu | |
ENST00000252242.8:c.506G>T | ENSP00000252242.4:p.Arg169Leu | |
ENST00000549420.1:c.176G>T | ENSP00000447209.1:p.Arg59Leu | |
ENST00000551275.1:c.401G>T | ENSP00000448041.1:p.Arg134Leu | |
ENST00000552629.5:n.604G>T | ||
NM_000424.3:c.506G>T | NP_000415.2:p.Arg169Leu | |
NM_000424.4:c.506G>T MANE Select | NP_000415.2:p.Arg169Leu |