HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240868515T>G , CM000664.2:g.240868515T>G | GRCh38 |
NC_000002.11:g.241807932T>G , CM000664.1:g.241807932T>G | GRCh37 |
NC_000002.10:g.241456605T>G | NCBI36 |
NG_008005.1:g.4771T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.3:c.-351T>G | ENSP00000302620.3:n.-351T>G | |
XR_924060.1:n.405+1718A>C |