Canonical Allele Identifier: CA500649684
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851185G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773819G>C , CM000679.2:g.46773819G>C GRCh38
NC_000017.10:g.44851185G>C , CM000679.1:g.44851185G>C GRCh37
NC_000017.9:g.42206348G>C NCBI36
NG_008084.2:g.49898C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-25C>G (WNT3) ENSP00000516418.1:n.-25C>G
ENST00000225512.6:c.171C>G (WNT3) MANE Select ENSP00000225512.5:p.Arg57=
ENST00000225512.5:c.171C>G (WNT3) ENSP00000225512.5:p.Arg57=
NM_030753.4:c.171C>G (WNT3) NP_110380.1:p.Arg57=
XM_024450773.1:c.4809+223300G>C (LRRC37A2) XP_024306541.1:n.4809+223300G>C
NM_030753.5:c.171C>G (WNT3) MANE Select NP_110380.1:p.Arg57=
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