HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99321782G>A , CM000666.2:g.99321782G>A | GRCh38 |
NC_000004.11:g.100242939G>A , CM000666.1:g.100242939G>A | GRCh37 |
NC_000004.10:g.100461962G>A | NCBI36 |
NG_011435.1:g.4634C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000639454.1:c.19-2896C>T | ENSP00000491622.1:n.19-2896C>T |