Canonical Allele Identifier: CA1739107547

Gene: WNT16

Linked Data

• dbSNP Id: rs1313358344

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121334786G>C , CM000669.2:g.121334786G>C	GRCh38
NC_000007.13:g.120974840G>C , CM000669.1:g.120974840G>C	GRCh37
NC_000007.12:g.120762076G>C	NCBI36
NG_029242.1:g.14420G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222462.3:c.633+2822G>C MANE Select	ENSP00000222462.2:n.633+2822G>C
ENST00000222462.2:c.633+2822G>C	ENSP00000222462.2:n.633+2822G>C
ENST00000361301.6:c.603+2822G>C	ENSP00000355065.2:n.603+2822G>C
NM_016087.2:c.603+2822G>C	NP_057171.2:n.603+2822G>C
NM_057168.1:c.633+2822G>C	NP_476509.1:n.633+2822G>C
NM_057168.2:c.633+2822G>C MANE Select	NP_476509.1:n.633+2822G>C