Canonical Allele Identifier: CA500649454
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851260G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773894G>C , CM000679.2:g.46773894G>C GRCh38
NC_000017.10:g.44851260G>C , CM000679.1:g.44851260G>C GRCh37
NC_000017.9:g.42206423G>C NCBI36
NG_008084.2:g.49823C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-100C>G (WNT3) ENSP00000516418.1:n.-100C>G
ENST00000225512.6:c.96C>G (WNT3) MANE Select ENSP00000225512.5:p.Gly32=
ENST00000225512.5:c.96C>G (WNT3) ENSP00000225512.5:p.Gly32=
ENST00000573788.5:n.507C>G (WNT3)
NM_030753.4:c.96C>G (WNT3) NP_110380.1:p.Gly32=
XM_024450773.1:c.4809+223375G>C (LRRC37A2) XP_024306541.1:n.4809+223375G>C
NM_030753.5:c.96C>G (WNT3) MANE Select NP_110380.1:p.Gly32=
Search 100 bp 5'
Search 100 bp 3'