Canonical Allele Identifier: CA351623248
Gene: WNT7A HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.13896205C>G (hg19) chr3:g.13854708C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854708C>G , CM000665.2:g.13854708C>G GRCh38
NC_000003.11:g.13896205C>G , CM000665.1:g.13896205C>G GRCh37
NC_000003.10:g.13871206C>G NCBI36
NG_008088.1:g.30414G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.394G>C MANE Select ENSP00000285018.4:p.Gly132Arg
ENST00000285018.4:c.394G>C ENSP00000285018.4:p.Gly132Arg
NM_004625.3:c.394G>C NP_004616.2:p.Gly132Arg
XM_011534090.1:c.193G>C XP_011532392.1:p.Gly65Arg
XM_011534091.1:c.193G>C XP_011532393.1:p.Gly65Arg
XM_011534091.2:c.193G>C XP_011532393.1:p.Gly65Arg
NM_004625.4:c.394G>C MANE Select NP_004616.2:p.Gly132Arg
Search 100 bp 5'
Search 100 bp 3'