Canonical Allele Identifier: CA15914325
Gene: WNT9B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11079740

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46871734G>C , CM000679.2:g.46871734G>C GRCh38
NC_000017.9:g.42304099G>C NCBI36
NC_000017.10:g.44949100G>C , CM000679.1:g.44949100G>C GRCh37
NG_029164.1:g.25133G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290015.6:c.78-783G>C ENSP00000290015.2:p.=
ENST00000393461.2:c.78-783G>C ENSP00000377105.2:p.=
ENST00000575372.5:c.96-783G>C ENSP00000458192.1:p.=
NM_003396.1:c.78-783G>C NP_003387.1:p.=
XM_005257637.2:c.78-783G>C XP_005257694.1:p.=
XM_011525178.1:c.96-783G>C XP_011523480.1:p.=