HGVS | Genome Assembly |
---|---|
NC_000013.11:g.30725416G= , CM000675.2:g.30725416G= | GRCh38 |
NC_000013.10:g.31299553G= , CM000675.1:g.31299553G= | GRCh37 |
NC_000013.9:g.30197553G= | NCBI36 |
NG_011963.2:g.16939G= |
HGVS | Amino-acid Change |
---|---|
NM_001204406.1:c.117-10135G= | NP_001191335.1:n.117-10135G= |
NM_001204406.2:c.117-10135G= | NP_001191335.1:n.117-10135G= |
ENST00000617770.4:c.117-10135G= | ENSP00000479870.1:n.117-10135G= |