HGVS | Genome Assembly |
---|---|
NC_000017.11:g.66240160C>T , CM000679.2:g.66240160C>T | GRCh38 |
NC_000017.10:g.64236278C>T , CM000679.1:g.64236278C>T | GRCh37 |
NC_000017.9:g.61666740C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000577982.1:c.-43-10738G>A | ENSP00000464301.1:n.-43-10738G>A |