HGVS | Genome Assembly |
---|---|
NC_000002.12:g.203866313G>T , CM000664.2:g.203866313G>T | GRCh38 |
NC_000002.11:g.204731036G>T , CM000664.1:g.204731036G>T | GRCh37 |
NC_000002.10:g.204439281G>T | NCBI36 |
NG_011502.1:g.3528G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696479.1:c.48-1605G>T | ENSP00000512655.1:n.48-1605G>T |