HGVS | Genome Assembly |
---|---|
NC_000006.12:g.106183905C>T , CM000668.2:g.106183905C>T | GRCh38 |
NC_000006.11:g.106631780C>T , CM000668.1:g.106631780C>T | GRCh37 |
NC_000006.10:g.106738473C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000636335.1:c.457+18067G>A | ENSP00000490221.1:n.457+18067G>A | |
ENST00000636437.1:c.457+18067G>A | ENSP00000490376.1:n.457+18067G>A |