HGVS | Genome Assembly |
---|---|
NC_000004.12:g.38810877T>A , CM000666.2:g.38810877T>A | GRCh38 |
NC_000004.11:g.38812498T>A , CM000666.1:g.38812498T>A | GRCh37 |
NC_000004.10:g.38488893T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506146.5:c.-352-5684A>T | ENSP00000423725.1:n.-352-5684A>T |