HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038456A>G , CM000666.2:g.52038456A>G | GRCh38 |
NC_000004.11:g.52904622A>G , CM000666.1:g.52904622A>G | GRCh37 |
NC_000004.10:g.52599379A>G | NCBI36 |
NG_008891.1:g.4864T>C , LRG_204:g.4864T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.9:c.-197T>C | ENSP00000370839.5:n.-197T>C |