HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038468T>C , CM000666.2:g.52038468T>C | GRCh38 |
NC_000004.11:g.52904634T>C , CM000666.1:g.52904634T>C | GRCh37 |
NC_000004.10:g.52599391T>C | NCBI36 |
NG_008891.1:g.4852A>G , LRG_204:g.4852A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.9:c.-209A>G | ENSP00000370839.5:n.-209A>G |