Canonical Allele Identifier: CA400011552
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773851A>G , CM000679.2:g.46773851A>G GRCh38
NC_000017.10:g.44851217A>G , CM000679.1:g.44851217A>G GRCh37
NC_000017.9:g.42206380A>G NCBI36
NG_008084.2:g.49866T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-57T>C (WNT3) ENSP00000516418.1:n.-57T>C
ENST00000225512.6:c.139T>C (WNT3) MANE Select ENSP00000225512.5:p.Ser47Pro
ENST00000225512.5:c.139T>C (WNT3) ENSP00000225512.5:p.Ser47Pro
ENST00000573788.5:n.550T>C (WNT3)
NM_030753.4:c.139T>C (WNT3) NP_110380.1:p.Ser47Pro
XM_024450773.1:c.4809+223332A>G (LRRC37A2) XP_024306541.1:n.4809+223332A>G
NM_030753.5:c.139T>C (WNT3) MANE Select NP_110380.1:p.Ser47Pro