HGVS | Genome Assembly |
---|---|
NC_000018.10:g.5856949T>C , CM000680.2:g.5856949T>C | GRCh38 |
NC_000018.9:g.5856948T>C , CM000680.1:g.5856948T>C | GRCh37 |
NC_000018.8:g.5846948T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_172494.1:n.603-21494T>C | ||
NR_172495.1:n.603-19304T>C | ||
NR_172496.1:n.603-19304T>C | ||
NR_172497.1:n.603-19304T>C | ||
NR_172498.1:n.663-10164T>C | ||
NR_172499.1:n.603-19304T>C | ||
NR_172500.1:n.603-19304T>C | ||
NR_172501.1:n.603-19304T>C | ||
NR_172502.1:n.603-19304T>C | ||
NR_172503.1:n.603-19304T>C |