Canonical Allele Identifier: CA400011199
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851058T>C (hg19) chr17:g.46773692T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773692T>C , CM000679.2:g.46773692T>C GRCh38
NC_000017.10:g.44851058T>C , CM000679.1:g.44851058T>C GRCh37
NC_000017.9:g.42206221T>C NCBI36
NG_008084.2:g.50025A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.103A>G (WNT3) ENSP00000516418.1:p.Ile35Val
ENST00000225512.6:c.298A>G (WNT3) MANE Select ENSP00000225512.5:p.Ile100Val
ENST00000225512.5:c.298A>G (WNT3) ENSP00000225512.5:p.Ile100Val
NM_030753.4:c.298A>G (WNT3) NP_110380.1:p.Ile100Val
XM_024450773.1:c.4809+223173T>C (LRRC37A2) XP_024306541.1:n.4809+223173T>C
NM_030753.5:c.298A>G (WNT3) MANE Select NP_110380.1:p.Ile100Val
Search 100 bp 5'
Search 100 bp 3'