Canonical Allele Identifier: CA15905385
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs199498

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46788237T>C , CM000679.2:g.46788237T>C GRCh38
NC_000017.10:g.44865603T>C , CM000679.1:g.44865603T>C GRCh37
NC_000017.9:g.42220763T>C NCBI36
NG_008084.2:g.35480A>G

Transcript Alleles

HGVS Amino-acid change
NM_030753.4:c.81-14328A>G (WNT3) VV NP_110380.1:p.=
XM_024450773.1:c.4809+237718T>C (LRRC37A2) XP_024306541.1:p.=
NM_030753.5:c.81-14328A>G (WNT3) VV NP_110380.1:p.=
ENST00000225512.5:c.81-14328A>G ENSP00000225512.5:p.=
ENST00000573788.5:n.492-14328A>G