Canonical Allele Identifier: CA351623234
Gene: WNT7A HGNC NCBI

Linked Data

dbSNP Id: rs546145028
gnomAD v4: 3-13854702-C-G
MyVariant Identifiers: chr3:g.13896199C>G (hg19) chr3:g.13854702C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854702C>G , CM000665.2:g.13854702C>G GRCh38
NC_000003.11:g.13896199C>G , CM000665.1:g.13896199C>G GRCh37
NC_000003.10:g.13871200C>G NCBI36
NG_008088.1:g.30420G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.400G>C MANE Select ENSP00000285018.4:p.Asp134His
ENST00000285018.4:c.400G>C ENSP00000285018.4:p.Asp134His
NM_004625.3:c.400G>C NP_004616.2:p.Asp134His
XM_011534090.1:c.199G>C XP_011532392.1:p.Asp67His
XM_011534091.1:c.199G>C XP_011532393.1:p.Asp67His
XM_011534091.2:c.199G>C XP_011532393.1:p.Asp67His
NM_004625.4:c.400G>C MANE Select NP_004616.2:p.Asp134His
Search 100 bp 5'
Search 100 bp 3'