HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29941940G>T , CM000668.2:g.29941940G>T | GRCh38 |
NC_000006.11:g.29909717G>T , CM000668.1:g.29909717G>T | GRCh37 |
NC_000006.10:g.30017696G>T | NCBI36 |
NG_029217.2:g.4478G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000396634.5:c.-281-26G>T | ENSP00000379873.1:n.-281-26G>T |