HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19484826T>C , CM000686.2:g.19484826T>C | GRCh38 |
NC_000024.9:g.21646712T>C , CM000686.1:g.21646712T>C | GRCh37 |
NC_000024.8:g.20106100T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650676.1:n.112-4532A>G | ||
ENST00000400605.5:n.106-4532A>G | ||
ENST00000441139.5:n.123-4532A>G | ||
ENST00000513194.1:n.59A>G | ||
NR_002923.2:n.123-4532A>G | ||
NR_033732.1:n.123-4532A>G |