HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99321802A>C , CM000666.2:g.99321802A>C | GRCh38 |
NC_000004.11:g.100242959A>C , CM000666.1:g.100242959A>C | GRCh37 |
NC_000004.10:g.100461982A>C | NCBI36 |
NG_011435.1:g.4614T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000639454.1:c.19-2916T>G | ENSP00000491622.1:n.19-2916T>G |