Canonical Allele Identifier: CA119261
Gene: WNT7A HGNC NCBI

Linked Data

ClinVar Variation Id: 8060
ClinVar RCV Id: RCV000008526
dbSNP Id: rs104893835
MyVariant Identifiers: chr3:g.13860617G>A (hg19) chr3:g.13819120G>A (hg38)
PubMed: PMID:16826533
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13819120G>A , CM000665.2:g.13819120G>A GRCh38
NC_000003.11:g.13860617G>A , CM000665.1:g.13860617G>A GRCh37
NC_000003.10:g.13835618G>A NCBI36
NG_008088.1:g.66002C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.874C>T MANE Select ENSP00000285018.4:p.Arg292Cys
ENST00000285018.4:c.874C>T ENSP00000285018.4:p.Arg292Cys
NM_004625.3:c.874C>T NP_004616.2:p.Arg292Cys
XM_011534090.1:c.673C>T XP_011532392.1:p.Arg225Cys
XM_011534091.1:c.673C>T XP_011532393.1:p.Arg225Cys
XM_011534091.2:c.673C>T XP_011532393.1:p.Arg225Cys
NM_004625.4:c.874C>T MANE Select NP_004616.2:p.Arg292Cys
Search 100 bp 5'
Search 100 bp 3'