HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19466550T>C , CM000686.2:g.19466550T>C | GRCh38 |
NC_000024.9:g.21628436T>C , CM000686.1:g.21628436T>C | GRCh37 |
NC_000024.8:g.20087824T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650676.1:n.1566A>G | ||
ENST00000400605.5:n.1560A>G | ||
ENST00000441139.5:n.1577A>G | ||
ENST00000513194.1:n.4473A>G | ||
NR_002923.2:n.1577A>G | ||
NR_033732.1:n.1577A>G |