Canonical Allele Identifier: CA500649500
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2694136
ClinVar RCV Id: RCV003544011
MyVariant Identifiers: chr17:g.44851038G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773672G>A , CM000679.2:g.46773672G>A GRCh38
NC_000017.10:g.44851038G>A , CM000679.1:g.44851038G>A GRCh37
NC_000017.9:g.42206201G>A NCBI36
NG_008084.2:g.50045C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.123C>T (WNT3) ENSP00000516418.1:p.Asp41=
ENST00000225512.6:c.318C>T (WNT3) MANE Select ENSP00000225512.5:p.Asp106=
ENST00000225512.5:c.318C>T (WNT3) ENSP00000225512.5:p.Asp106=
NM_030753.4:c.318C>T (WNT3) NP_110380.1:p.Asp106=
XM_024450773.1:c.4809+223153G>A (LRRC37A2) XP_024306541.1:n.4809+223153G>A
NM_030753.5:c.318C>T (WNT3) MANE Select NP_110380.1:p.Asp106=
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