HGVS | Genome Assembly |
---|---|
NC_000016.10:g.74774272G>T , CM000678.2:g.74774272G>T | GRCh38 |
NC_000016.9:g.74808170G>T , CM000678.1:g.74808170G>T | GRCh37 |
NC_000016.8:g.73365671G>T | NCBI36 |
NG_017070.1:g.5560C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219368.8:c.270+214C>A MANE Select | ENSP00000219368.3:n.270+214C>A | |
ENST00000219368.7:c.270+214C>A | ENSP00000219368.3:n.270+214C>A | |
ENST00000567683.5:c.270+214C>A | ENSP00000455126.1:n.270+214C>A | |
NM_024306.4:c.270+214C>A | NP_077282.3:n.270+214C>A | |
XM_011523317.1:c.270+214C>A | XP_011521619.1:n.270+214C>A | |
XM_011523318.1:c.270+214C>A | XP_011521620.1:n.270+214C>A | |
XM_011523317.3:c.270+214C>A | XP_011521619.1:n.270+214C>A | |
NM_024306.5:c.270+214C>A MANE Select | NP_077282.3:n.270+214C>A |