Canonical Allele Identifier: CA14404647
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs199515

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46779275G>C , CM000679.2:g.46779275G>C GRCh38
NC_000017.10:g.44856641G>C , CM000679.1:g.44856641G>C GRCh37
NG_008084.2:g.44442C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.-115-5366C>G (WNT3) ENSP00000516418.1:n.-115-5366C>G
ENST00000225512.6:c.81-5366C>G (WNT3) MANE Select ENSP00000225512.5:n.81-5366C>G
ENST00000225512.5:c.81-5366C>G (WNT3) ENSP00000225512.5:n.81-5366C>G
ENST00000573788.5:n.492-5366C>G (WNT3)
NM_030753.4:c.81-5366C>G (WNT3) NP_110380.1:n.81-5366C>G
XM_024450773.1:c.4809+228756G>C (LRRC37A2) XP_024306541.1:n.4809+228756G>C
NM_030753.5:c.81-5366C>G (WNT3) MANE Select NP_110380.1:n.81-5366C>G