Canonical Allele Identifier: CA400011157
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773672G>T , CM000679.2:g.46773672G>T GRCh38
NC_000017.10:g.44851038G>T , CM000679.1:g.44851038G>T GRCh37
NC_000017.9:g.42206201G>T NCBI36
NG_008084.2:g.50045C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.123C>A (WNT3) ENSP00000516418.1:p.Asp41Glu
ENST00000225512.6:c.318C>A (WNT3) MANE Select ENSP00000225512.5:p.Asp106Glu
ENST00000225512.5:c.318C>A (WNT3) ENSP00000225512.5:p.Asp106Glu
NM_030753.4:c.318C>A (WNT3) NP_110380.1:p.Asp106Glu
XM_024450773.1:c.4809+223153G>T (LRRC37A2) XP_024306541.1:n.4809+223153G>T
NM_030753.5:c.318C>A (WNT3) MANE Select NP_110380.1:p.Asp106Glu