HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52520501C>A , CM000674.2:g.52520501C>A | GRCh38 |
NC_000012.11:g.52914285C>A , CM000674.1:g.52914285C>A | GRCh37 |
NC_000012.10:g.51200552C>A | NCBI36 |
NG_008297.1:g.4959G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.8:c.-205G>T | ENSP00000252242.4:n.-205G>T | |
ENST00000546577.1:c.-117G>T | ENSP00000449651.1:n.-117G>T |