Canonical Allele Identifier: CA400011600
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851241C>A (hg19) chr17:g.46773875C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773875C>A , CM000679.2:g.46773875C>A GRCh38
NC_000017.10:g.44851241C>A , CM000679.1:g.44851241C>A GRCh37
NC_000017.9:g.42206404C>A NCBI36
NG_008084.2:g.49842G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-81G>T (WNT3) ENSP00000516418.1:n.-81G>T
ENST00000225512.6:c.115G>T (WNT3) MANE Select ENSP00000225512.5:p.Gly39Cys
ENST00000225512.5:c.115G>T (WNT3) ENSP00000225512.5:p.Gly39Cys
ENST00000573788.5:n.526G>T (WNT3)
NM_030753.4:c.115G>T (WNT3) NP_110380.1:p.Gly39Cys
XM_024450773.1:c.4809+223356C>A (LRRC37A2) XP_024306541.1:n.4809+223356C>A
NM_030753.5:c.115G>T (WNT3) MANE Select NP_110380.1:p.Gly39Cys
Search 100 bp 5'
Search 100 bp 3'