HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038434C>A , CM000666.2:g.52038434C>A | GRCh38 |
NC_000004.11:g.52904600C>A , CM000666.1:g.52904600C>A | GRCh37 |
NC_000004.10:g.52599357C>A | NCBI36 |
NG_008891.1:g.4886G>T , LRG_204:g.4886G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.9:c.-175G>T | ENSP00000370839.5:n.-175G>T |