HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44359342T>A , CM000667.2:g.44359342T>A | GRCh38 |
NC_000005.9:g.44359444T>A , CM000667.1:g.44359444T>A | GRCh37 |
NC_000005.8:g.44395201T>A | NCBI36 |
NG_011446.1:g.34341A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.325+29016A>T MANE Select | ENSP00000264664.4:n.325+29016A>T | |
ENST00000264664.4:c.325+29016A>T | ENSP00000264664.4:n.325+29016A>T | |
NM_004465.1:c.325+29016A>T | NP_004456.1:n.325+29016A>T | |
XM_005248264.2:c.325+29016A>T | XP_005248321.1:n.325+29016A>T | |
XM_005248264.4:c.325+29016A>T | XP_005248321.1:n.325+29016A>T | |
NM_004465.2:c.325+29016A>T MANE Select | NP_004456.1:n.325+29016A>T |