Canonical Allele Identifier: CA4455637
Gene: WNT16 HGNC NCBI
COSMIC:
COSM1599875 (not active)
COSM1599876 (not active)
MyVariant.info:
GRCh38 chr7:g.121329715G>A
GRCh37 chr7:g.120969769G>A
Revel Score:
ENST00000361301 0.170
ENST00000222462 (MANE Select) 0.170
ENST00000414945 0.170
gnomAD v2:
7:120969769 G / A
gnomAD v3:
7:121329715 G / A
gnomAD v4:
chr7-121329715-G-A
Joint Max Group AF 0.84755189 (AFR)
Genomes Max Group AF 0.83707852 (AFR)
Exomes Max Group AF 0.85543145 (AFR)
dbSNP:
2908004
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121329715G>A , CM000669.2:g.121329715G>A GRCh38
NC_000007.13:g.120969769G>A , CM000669.1:g.120969769G>A GRCh37
NC_000007.12:g.120757005G>A NCBI36
NG_029242.1:g.9349G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222462.3:c.244G>A MANE Select ENSP00000222462.2:p.Gly82Arg
ENST00000222462.2:c.244G>A ENSP00000222462.2:p.Gly82Arg
ENST00000361301.6:c.214G>A ENSP00000355065.2:p.Gly72Arg
NM_016087.2:c.214G>A NP_057171.2:p.Gly72Arg
NM_057168.1:c.244G>A NP_476509.1:p.Gly82Arg
NM_057168.2:c.244G>A MANE Select NP_476509.1:p.Gly82Arg
Search 100 bp 5'
Search 100 bp 3'