HGVS | Genome Assembly |
---|---|
NC_000013.11:g.30731035G= , CM000675.2:g.30731035G= | GRCh38 |
NC_000013.10:g.31305172G= , CM000675.1:g.31305172G= | GRCh37 |
NC_000013.9:g.30203172G= | NCBI36 |
NG_011963.2:g.22558G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000617770.4:c.117-4516G= | ENSP00000479870.1:n.117-4516G= | |
NM_001204406.1:c.117-4516G= | NP_001191335.1:n.117-4516G= | |
NM_001204406.2:c.117-4516G= | NP_001191335.1:n.117-4516G= |