HGVS | Genome Assembly |
---|---|
NC_000002.12:g.217506478C= , CM000664.2:g.217506478C= | GRCh38 |
NC_000002.11:g.218371201C= , CM000664.1:g.218371201C= | GRCh37 |
NC_000002.10:g.218079446C= | NCBI36 |
HGVS | Amino-acid Change |
---|---|
NR_026597.1:n.1345-27920G= | |
NR_026597.2:n.1345-27920G= | |
ENST00000474063.5:n.322-27920G= | |
ENST00000486365.5:n.1345-27920G= |