Canonical Allele Identifier: CA400011391
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851144T>G (hg19) chr17:g.46773778T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773778T>G , CM000679.2:g.46773778T>G GRCh38
NC_000017.10:g.44851144T>G , CM000679.1:g.44851144T>G GRCh37
NC_000017.9:g.42206307T>G NCBI36
NG_008084.2:g.49939A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.17A>C (WNT3) ENSP00000516418.1:p.Glu6Ala
ENST00000225512.6:c.212A>C (WNT3) MANE Select ENSP00000225512.5:p.Glu71Ala
ENST00000225512.5:c.212A>C (WNT3) ENSP00000225512.5:p.Glu71Ala
NM_030753.4:c.212A>C (WNT3) NP_110380.1:p.Glu71Ala
XM_024450773.1:c.4809+223259T>G (LRRC37A2) XP_024306541.1:n.4809+223259T>G
NM_030753.5:c.212A>C (WNT3) MANE Select NP_110380.1:p.Glu71Ala
Search 100 bp 5'
Search 100 bp 3'