HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52520318C>A , CM000674.2:g.52520318C>A | GRCh38 |
NC_000012.11:g.52914102C>A , CM000674.1:g.52914102C>A | GRCh37 |
NC_000012.10:g.51200369C>A | NCBI36 |
NG_008297.1:g.5142G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252242.9:c.-22G>T MANE Select | ENSP00000252242.4:n.-22G>T | |
ENST00000252242.8:c.-22G>T | ENSP00000252242.4:n.-22G>T | |
ENST00000546577.1:c.-12-10G>T | ENSP00000449651.1:n.-12-10G>T | |
ENST00000549420.1:c.-22G>T | ENSP00000447209.1:n.-22G>T | |
ENST00000551275.1:c.-22G>T | ENSP00000448041.1:n.-22G>T | |
ENST00000552629.5:n.77G>T | ||
NM_000424.3:c.-22G>T | NP_000415.2:n.-22G>T | |
NM_000424.4:c.-22G>T MANE Select | NP_000415.2:n.-22G>T |