Canonical Allele Identifier: CA400011646
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851264A>T (hg19) chr17:g.46773898A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773898A>T , CM000679.2:g.46773898A>T GRCh38
NC_000017.10:g.44851264A>T , CM000679.1:g.44851264A>T GRCh37
NC_000017.9:g.42206427A>T NCBI36
NG_008084.2:g.49819T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-104T>A (WNT3) ENSP00000516418.1:n.-104T>A
ENST00000225512.6:c.92T>A (WNT3) MANE Select ENSP00000225512.5:p.Leu31Gln
ENST00000225512.5:c.92T>A (WNT3) ENSP00000225512.5:p.Leu31Gln
ENST00000573788.5:n.503T>A (WNT3)
NM_030753.4:c.92T>A (WNT3) NP_110380.1:p.Leu31Gln
XM_024450773.1:c.4809+223379A>T (LRRC37A2) XP_024306541.1:n.4809+223379A>T
NM_030753.5:c.92T>A (WNT3) MANE Select NP_110380.1:p.Leu31Gln
Search 100 bp 5'
Search 100 bp 3'