Canonical Allele Identifier: CA2262378201
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773906G= , CM000679.2:g.46773906G= GRCh38
NC_000017.10:g.44851272G= , CM000679.1:g.44851272G= GRCh37
NC_000017.9:g.42206435G= NCBI36
NG_008084.2:g.49811C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-112C= (WNT3) ENSP00000516418.1:n.-112C=
ENST00000225512.6:c.84C= (WNT3) MANE Select ENSP00000225512.5:p.Ser28=
ENST00000225512.5:c.84C= (WNT3) ENSP00000225512.5:p.Ser28=
ENST00000573788.5:n.495C= (WNT3)
NM_030753.4:c.84C= (WNT3) NP_110380.1:p.Ser28=
XM_024450773.1:c.4809+223387G= (LRRC37A2) XP_024306541.1:n.4809+223387G=
NM_030753.5:c.84C= (WNT3) MANE Select NP_110380.1:p.Ser28=
Search 100 bp 5'
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