HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038381C>G , CM000666.2:g.52038381C>G | GRCh38 |
NC_000004.11:g.52904547C>G , CM000666.1:g.52904547C>G | GRCh37 |
NC_000004.10:g.52599304C>G | NCBI36 |
NG_008891.1:g.4939G>C , LRG_204:g.4939G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.9:c.-122G>C | ENSP00000370839.5:n.-122G>C |