Canonical Allele Identifier: CA12519585
Gene: WNT16 HGNC NCBI

Linked Data

dbSNP Id: rs3801387
gnomAD v2: 7-120974765-A-G
gnomAD v3: 7-121334711-A-G
gnomAD v4: 7-121334711-A-G
MyVariant Identifiers: chr7:g.120974765A>G (hg19) chr7:g.121334711A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121334711A>G , CM000669.2:g.121334711A>G GRCh38
NC_000007.13:g.120974765A>G , CM000669.1:g.120974765A>G GRCh37
NC_000007.12:g.120762001A>G NCBI36
NG_029242.1:g.14345A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222462.3:c.633+2747A>G MANE Select ENSP00000222462.2:n.633+2747A>G
ENST00000222462.2:c.633+2747A>G ENSP00000222462.2:n.633+2747A>G
ENST00000361301.6:c.603+2747A>G ENSP00000355065.2:n.603+2747A>G
NM_016087.2:c.603+2747A>G NP_057171.2:n.603+2747A>G
NM_057168.1:c.633+2747A>G NP_476509.1:n.633+2747A>G
NM_057168.2:c.633+2747A>G MANE Select NP_476509.1:n.633+2747A>G
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