Canonical Allele Identifier: CA2266483
Gene: WNT7A HGNC NCBI

Linked Data

dbSNP Id: rs753785082
ExAC: 3:13896285 G / A
gnomAD v2: 3-13896285-G-A
gnomAD v4: 3-13854788-G-A
COSMIC: COSM1270515
MyVariant Identifiers: chr3:g.13896285G>A (hg19) chr3:g.13854788G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854788G>A , CM000665.2:g.13854788G>A GRCh38
NC_000003.11:g.13896285G>A , CM000665.1:g.13896285G>A GRCh37
NC_000003.10:g.13871286G>A NCBI36
NG_008088.1:g.30334C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.314C>T MANE Select ENSP00000285018.4:p.Ala105Val
ENST00000285018.4:c.314C>T ENSP00000285018.4:p.Ala105Val
NM_004625.3:c.314C>T NP_004616.2:p.Ala105Val
XM_011534090.1:c.113C>T XP_011532392.1:p.Ala38Val
XM_011534091.1:c.113C>T XP_011532393.1:p.Ala38Val
XM_011534091.2:c.113C>T XP_011532393.1:p.Ala38Val
NM_004625.4:c.314C>T MANE Select NP_004616.2:p.Ala105Val
Search 100 bp 5'
Search 100 bp 3'