HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29941969C>G , CM000668.2:g.29941969C>G | GRCh38 |
NC_000006.11:g.29909746C>G , CM000668.1:g.29909746C>G | GRCh37 |
NC_000006.10:g.30017725C>G | NCBI36 |
NG_029217.2:g.4507C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000396634.5:c.-278C>G | ENSP00000379873.1:n.-278C>G |