Canonical Allele Identifier: CA400011640
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.44851259G>T (hg19) chr17:g.46773893G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773893G>T , CM000679.2:g.46773893G>T GRCh38
NC_000017.10:g.44851259G>T , CM000679.1:g.44851259G>T GRCh37
NC_000017.9:g.42206422G>T NCBI36
NG_008084.2:g.49824C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-99C>A (WNT3) ENSP00000516418.1:n.-99C>A
ENST00000225512.6:c.97C>A (WNT3) MANE Select ENSP00000225512.5:p.Gln33Lys
ENST00000225512.5:c.97C>A (WNT3) ENSP00000225512.5:p.Gln33Lys
ENST00000573788.5:n.508C>A (WNT3)
NM_030753.4:c.97C>A (WNT3) NP_110380.1:p.Gln33Lys
XM_024450773.1:c.4809+223374G>T (LRRC37A2) XP_024306541.1:n.4809+223374G>T
NM_030753.5:c.97C>A (WNT3) MANE Select NP_110380.1:p.Gln33Lys
Search 100 bp 5'
Search 100 bp 3'