Canonical Allele Identifier: CA2266478

Gene: WNT7A

Linked Data

• dbSNP Id: rs531986676
• ExAC: 3:13896278 G / A
• gnomAD v2: 3-13896278-G-A
• gnomAD v3: 3-13854781-G-A
• gnomAD v4: 3-13854781-G-A
• MyVariant Identifiers: chr3:g.13896278G>A (hg19) ; chr3:g.13854781G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854781G>A , CM000665.2:g.13854781G>A	GRCh38
NC_000003.11:g.13896278G>A , CM000665.1:g.13896278G>A	GRCh37
NC_000003.10:g.13871279G>A	NCBI36
NG_008088.1:g.30341C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000285018.5:c.321C>T MANE Select	ENSP00000285018.4:p.Thr107=
ENST00000285018.4:c.321C>T	ENSP00000285018.4:p.Thr107=
NM_004625.3:c.321C>T	NP_004616.2:p.Thr107=
XM_011534090.1:c.120C>T	XP_011532392.1:p.Thr40=
XM_011534091.1:c.120C>T	XP_011532393.1:p.Thr40=
XM_011534091.2:c.120C>T	XP_011532393.1:p.Thr40=
NM_004625.4:c.321C>T MANE Select	NP_004616.2:p.Thr107=