Canonical Allele Identifier: CA165899427
Gene: WNT16 HGNC NCBI

Linked Data

dbSNP Id: rs777854034
gnomAD v3: 7-121334791-G-A
gnomAD v4: 7-121334791-G-A
MyVariant Identifiers: chr7:g.120974845G>A (hg19) chr7:g.121334791G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121334791G>A , CM000669.2:g.121334791G>A GRCh38
NC_000007.13:g.120974845G>A , CM000669.1:g.120974845G>A GRCh37
NC_000007.12:g.120762081G>A NCBI36
NG_029242.1:g.14425G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222462.3:c.633+2827G>A MANE Select ENSP00000222462.2:n.633+2827G>A
ENST00000222462.2:c.633+2827G>A ENSP00000222462.2:n.633+2827G>A
ENST00000361301.6:c.603+2827G>A ENSP00000355065.2:n.603+2827G>A
NM_016087.2:c.603+2827G>A NP_057171.2:n.603+2827G>A
NM_057168.1:c.633+2827G>A NP_476509.1:n.633+2827G>A
NM_057168.2:c.633+2827G>A MANE Select NP_476509.1:n.633+2827G>A
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