HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157114880A>T , CM000667.2:g.157114880A>T | GRCh38 |
NC_000005.9:g.156541891A>T , CM000667.1:g.156541891A>T | GRCh37 |
NC_000005.8:g.156474469A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524219.2:c.-293-7918T>A | ENSP00000430328.2:n.-293-7918T>A | |
ENST00000524219.1:c.-293-7918T>A | ENSP00000430328.1:n.-293-7918T>A |