HGVS | Genome Assembly |
---|---|
NC_000002.12:g.201287915T>G , CM000664.2:g.201287915T>G | GRCh38 |
NC_000002.11:g.202152638T>G , CM000664.1:g.202152638T>G | GRCh37 |
NC_000002.10:g.201860883T>G | NCBI36 |
NG_007497.1:g.59458T>G , LRG_34:g.59458T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696069.1:c.1259+2598T>G | ENSP00000512371.1:n.1259+2598T>G |