HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6471049C>T , CM000674.2:g.6471049C>T | GRCh38 |
NC_000012.11:g.6580215C>T , CM000674.1:g.6580215C>T | GRCh37 |
NC_000012.10:g.6450476C>T | NCBI36 |
NG_042188.1:g.4851G>A | |
NG_042188.2:g.4851G>A |
HGVS | Amino-acid Change | |
---|---|---|
XR_001748777.2:n.2316C>T | ||
XR_001748778.2:n.2313C>T |