Canonical Allele Identifier: CA351623408
Gene: WNT7A HGNC NCBI

Linked Data

dbSNP Id: rs1575068969
MyVariant Identifiers: chr3:g.13896282A>G (hg19) chr3:g.13854785A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854785A>G , CM000665.2:g.13854785A>G GRCh38
NC_000003.11:g.13896282A>G , CM000665.1:g.13896282A>G GRCh37
NC_000003.10:g.13871283A>G NCBI36
NG_008088.1:g.30337T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.317T>C MANE Select ENSP00000285018.4:p.Phe106Ser
ENST00000285018.4:c.317T>C ENSP00000285018.4:p.Phe106Ser
NM_004625.3:c.317T>C NP_004616.2:p.Phe106Ser
XM_011534090.1:c.116T>C XP_011532392.1:p.Phe39Ser
XM_011534091.1:c.116T>C XP_011532393.1:p.Phe39Ser
XM_011534091.2:c.116T>C XP_011532393.1:p.Phe39Ser
NM_004625.4:c.317T>C MANE Select NP_004616.2:p.Phe106Ser
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