HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44305751C>A , CM000667.2:g.44305751C>A | GRCh38 |
NC_000005.9:g.44305853C>A , CM000667.1:g.44305853C>A | GRCh37 |
NC_000005.8:g.44341610C>A | NCBI36 |
NG_011446.1:g.87932G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.430-559G>T MANE Select | ENSP00000264664.4:n.430-559G>T | |
ENST00000264664.4:c.430-559G>T | ENSP00000264664.4:n.430-559G>T | |
NM_004465.1:c.430-559G>T | NP_004456.1:n.430-559G>T | |
XM_005248264.2:c.430-559G>T | XP_005248321.1:n.430-559G>T | |
XM_005248264.4:c.430-559G>T | XP_005248321.1:n.430-559G>T | |
NM_004465.2:c.430-559G>T MANE Select | NP_004456.1:n.430-559G>T |