Canonical Allele Identifier: CA400011430
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851161G>C (hg19) chr17:g.46773795G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773795G>C , CM000679.2:g.46773795G>C GRCh38
NC_000017.10:g.44851161G>C , CM000679.1:g.44851161G>C GRCh37
NC_000017.9:g.42206324G>C NCBI36
NG_008084.2:g.49922C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-1C>G (WNT3) ENSP00000516418.1:n.-1C>G
ENST00000225512.6:c.195C>G (WNT3) MANE Select ENSP00000225512.5:p.Ile65Met
ENST00000225512.5:c.195C>G (WNT3) ENSP00000225512.5:p.Ile65Met
NM_030753.4:c.195C>G (WNT3) NP_110380.1:p.Ile65Met
XM_024450773.1:c.4809+223276G>C (LRRC37A2) XP_024306541.1:n.4809+223276G>C
NM_030753.5:c.195C>G (WNT3) MANE Select NP_110380.1:p.Ile65Met
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