HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44359341A= , CM000667.2:g.44359341A= | GRCh38 |
NC_000005.9:g.44359443A= , CM000667.1:g.44359443A= | GRCh37 |
NC_000005.8:g.44395200A= | NCBI36 |
NG_011446.1:g.34342T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.325+29017T= MANE Select | ENSP00000264664.4:n.325+29017T= | |
ENST00000264664.4:c.325+29017T= | ENSP00000264664.4:n.325+29017T= | |
NM_004465.1:c.325+29017T= | NP_004456.1:n.325+29017T= | |
XM_005248264.2:c.325+29017T= | XP_005248321.1:n.325+29017T= | |
XM_005248264.4:c.325+29017T= | XP_005248321.1:n.325+29017T= | |
NM_004465.2:c.325+29017T= MANE Select | NP_004456.1:n.325+29017T= |