Canonical Allele Identifier: CA500649561
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851086G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773720G>A , CM000679.2:g.46773720G>A GRCh38
NC_000017.10:g.44851086G>A , CM000679.1:g.44851086G>A GRCh37
NC_000017.9:g.42206249G>A NCBI36
NG_008084.2:g.49997C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.75C>T (WNT3) ENSP00000516418.1:p.Asn25=
ENST00000225512.6:c.270C>T (WNT3) MANE Select ENSP00000225512.5:p.Asn90=
ENST00000225512.5:c.270C>T (WNT3) ENSP00000225512.5:p.Asn90=
NM_030753.4:c.270C>T (WNT3) NP_110380.1:p.Asn90=
XM_024450773.1:c.4809+223201G>A (LRRC37A2) XP_024306541.1:n.4809+223201G>A
NM_030753.5:c.270C>T (WNT3) MANE Select NP_110380.1:p.Asn90=
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