Canonical Allele Identifier: CA400011567
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773859A>C , CM000679.2:g.46773859A>C GRCh38
NC_000017.10:g.44851225A>C , CM000679.1:g.44851225A>C GRCh37
NC_000017.9:g.42206388A>C NCBI36
NG_008084.2:g.49858T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-65T>G (WNT3) ENSP00000516418.1:n.-65T>G
ENST00000225512.6:c.131T>G (WNT3) MANE Select ENSP00000225512.5:p.Leu44Arg
ENST00000225512.5:c.131T>G (WNT3) ENSP00000225512.5:p.Leu44Arg
ENST00000573788.5:n.542T>G (WNT3)
NM_030753.4:c.131T>G (WNT3) NP_110380.1:p.Leu44Arg
XM_024450773.1:c.4809+223340A>C (LRRC37A2) XP_024306541.1:n.4809+223340A>C
NM_030753.5:c.131T>G (WNT3) MANE Select NP_110380.1:p.Leu44Arg