HGVS | Genome Assembly |
---|---|
NC_000007.14:g.45921476G>T , CM000669.2:g.45921476G>T | GRCh38 |
NC_000007.13:g.45961075G>T , CM000669.1:g.45961075G>T | GRCh37 |
NC_000007.12:g.45927600G>T | NCBI36 |
NG_011508.1:g.4797C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000448817.1:c.73+151C>A | ENSP00000389668.1:n.73+151C>A |