Canonical Allele Identifier: CA291163113
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs939897615
gnomAD v3: 17-46773887-A-G
gnomAD v4: 17-46773887-A-G
MyVariant Identifiers: chr17:g.44851253A>G (hg19) chr17:g.46773887A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773887A>G , CM000679.2:g.46773887A>G GRCh38
NC_000017.10:g.44851253A>G , CM000679.1:g.44851253A>G GRCh37
NC_000017.9:g.42206416A>G NCBI36
NG_008084.2:g.49830T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-93T>C (WNT3) ENSP00000516418.1:n.-93T>C
ENST00000225512.6:c.103T>C (WNT3) MANE Select ENSP00000225512.5:p.Tyr35His
ENST00000225512.5:c.103T>C (WNT3) ENSP00000225512.5:p.Tyr35His
ENST00000573788.5:n.514T>C (WNT3)
NM_030753.4:c.103T>C (WNT3) NP_110380.1:p.Tyr35His
XM_024450773.1:c.4809+223368A>G (LRRC37A2) XP_024306541.1:n.4809+223368A>G
NM_030753.5:c.103T>C (WNT3) MANE Select NP_110380.1:p.Tyr35His
Search 100 bp 5'
Search 100 bp 3'