Canonical Allele Identifier: CA2266464
Gene: WNT7A HGNC NCBI

Linked Data

dbSNP Id: rs752165682
ExAC: 3:13896239 T / A
gnomAD v2: 3-13896239-T-A
gnomAD v4: 3-13854742-T-A
MyVariant Identifiers: chr3:g.13896239T>A (hg19) chr3:g.13854742T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854742T>A , CM000665.2:g.13854742T>A GRCh38
NC_000003.11:g.13896239T>A , CM000665.1:g.13896239T>A GRCh37
NC_000003.10:g.13871240T>A NCBI36
NG_008088.1:g.30380A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.360A>T MANE Select ENSP00000285018.4:p.Thr120=
ENST00000285018.4:c.360A>T ENSP00000285018.4:p.Thr120=
NM_004625.3:c.360A>T NP_004616.2:p.Thr120=
XM_011534090.1:c.159A>T XP_011532392.1:p.Thr53=
XM_011534091.1:c.159A>T XP_011532393.1:p.Thr53=
XM_011534091.2:c.159A>T XP_011532393.1:p.Thr53=
NM_004625.4:c.360A>T MANE Select NP_004616.2:p.Thr120=
Search 100 bp 5'
Search 100 bp 3'