HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44335700T= , CM000667.2:g.44335700T= | GRCh38 |
NC_000005.9:g.44335802T= , CM000667.1:g.44335802T= | GRCh37 |
NC_000005.8:g.44371559T= | NCBI36 |
NG_011446.1:g.57983A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.326-25170A= MANE Select | ENSP00000264664.4:n.326-25170A= | |
ENST00000264664.4:c.326-25170A= | ENSP00000264664.4:n.326-25170A= | |
NM_004465.1:c.326-25170A= | NP_004456.1:n.326-25170A= | |
XM_005248264.2:c.326-25170A= | XP_005248321.1:n.326-25170A= | |
XM_005248264.4:c.326-25170A= | XP_005248321.1:n.326-25170A= | |
NM_004465.2:c.326-25170A= MANE Select | NP_004456.1:n.326-25170A= |