HGVS | Genome Assembly |
---|---|
NC_000016.10:g.84032263A= , CM000678.2:g.84032263A= | GRCh38 |
NC_000016.9:g.84065868A= , CM000678.1:g.84065868A= | GRCh37 |
NC_000016.8:g.82623369A= | NCBI36 |
NG_034136.1:g.14895T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299709.8:c.531-295T= MANE Select | ENSP00000299709.3:n.531-295T= | |
ENST00000299709.7:c.531-295T= | ENSP00000299709.3:n.531-295T= | |
ENST00000568178.1:c.531-295T= | ENSP00000457737.1:n.531-295T= | |
NM_001080442.2:c.531-295T= | NP_001073911.1:n.531-295T= | |
XM_011522872.1:c.531-295T= | XP_011521174.1:n.531-295T= | |
XM_017022946.1:c.531-295T= | XP_016878435.1:n.531-295T= | |
NM_001080442.3:c.531-295T= MANE Select | NP_001073911.1:n.531-295T= |