HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275249C>A , CM000672.2:g.80275249C>A | GRCh38 |
NC_000010.10:g.82035005C>A , CM000672.1:g.82035005C>A | GRCh37 |
NC_000010.9:g.82024985C>A | NCBI36 |
NG_008083.1:g.19430G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.769-50G>T MANE Select | ENSP00000361287.3:n.769-50G>T | |
ENST00000372213.7:c.769-50G>T | ENSP00000361287.3:n.769-50G>T | |
ENST00000485270.5:n.231G>T | ||
NM_000429.2:c.769-50G>T | NP_000420.1:n.769-50G>T | |
XM_005269842.3:c.769-50G>T | XP_005269899.1:n.769-50G>T | |
XM_005269843.3:c.646-50G>T | XP_005269900.1:n.646-50G>T | |
NM_000429.3:c.769-50G>T MANE Select | NP_000420.1:n.769-50G>T |