HGVS | Genome Assembly |
---|---|
NC_000002.12:g.217041003C>T , CM000664.2:g.217041003C>T | GRCh38 |
NC_000002.11:g.217905726C>T , CM000664.1:g.217905726C>T | GRCh37 |
NC_000002.10:g.217613971C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XR_923881.1:n.299+46985C>T | ||
XR_923883.1:n.294+46985C>T | ||
XR_923885.1:n.862+46985C>T | ||
XR_923886.1:n.359-14188C>T | ||
XR_923887.1:n.300-14188C>T | ||
XR_001739169.1:n.11844+46985C>T | ||
XR_001739170.2:n.8480+46985C>T | ||
XR_001739171.2:n.8347+46985C>T | ||
XR_923878.2:n.7316C>T |