HGVS | Genome Assembly |
---|---|
NC_000010.11:g.44386425C>T , CM000672.2:g.44386425C>T | GRCh38 |
NC_000010.10:g.44881873C>T , CM000672.1:g.44881873C>T | GRCh37 |
NC_000010.9:g.44201879C>T | NCBI36 |
NG_016861.1:g.3673G>A | |
NG_016861.2:g.3673G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496375.1:n.69G>A |