Canonical Allele Identifier: CA2266481
Gene: WNT7A HGNC NCBI

Linked Data

dbSNP Id: rs755662911
ExAC: 3:13896281 G / A
gnomAD v2: 3-13896281-G-A
MyVariant Identifiers: chr3:g.13896281G>A (hg19) chr3:g.13854784G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854784G>A , CM000665.2:g.13854784G>A GRCh38
NC_000003.11:g.13896281G>A , CM000665.1:g.13896281G>A GRCh37
NC_000003.10:g.13871282G>A NCBI36
NG_008088.1:g.30338C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.318C>T MANE Select ENSP00000285018.4:p.Phe106=
ENST00000285018.4:c.318C>T ENSP00000285018.4:p.Phe106=
NM_004625.3:c.318C>T NP_004616.2:p.Phe106=
XM_011534090.1:c.117C>T XP_011532392.1:p.Phe39=
XM_011534091.1:c.117C>T XP_011532393.1:p.Phe39=
XM_011534091.2:c.117C>T XP_011532393.1:p.Phe39=
NM_004625.4:c.318C>T MANE Select NP_004616.2:p.Phe106=
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