HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038461C>A , CM000666.2:g.52038461C>A | GRCh38 |
NC_000004.11:g.52904627C>A , CM000666.1:g.52904627C>A | GRCh37 |
NC_000004.10:g.52599384C>A | NCBI36 |
NG_008891.1:g.4859G>T , LRG_204:g.4859G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.9:c.-202G>T | ENSP00000370839.5:n.-202G>T |