HGVS | Genome Assembly |
---|---|
NC_000010.11:g.79425586T>A , CM000672.2:g.79425586T>A | GRCh38 |
NC_000010.10:g.81185342T>A , CM000672.1:g.81185342T>A | GRCh37 |
NC_000010.9:g.80855348T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372336.4:c.447+6972A>T MANE Select | ENSP00000361411.3:n.447+6972A>T | |
ENST00000372333.3:c.268+6972A>T | ENSP00000361408.3:n.268+6972A>T | |
ENST00000372336.3:c.447+6972A>T | ENSP00000361411.3:n.447+6972A>T | |
NM_153367.3:c.447+6972A>T | NP_699198.2:n.447+6972A>T | |
XM_011539452.1:c.237+6972A>T | XP_011537754.1:n.237+6972A>T | |
XM_011539452.3:c.237+6972A>T | XP_011537754.1:n.237+6972A>T | |
NM_153367.4:c.447+6972A>T MANE Select | NP_699198.2:n.447+6972A>T |