Canonical Allele Identifier: CA850505176

Gene: FZD3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28557160C>A , CM000670.2:g.28557160C>A	GRCh38
NC_000008.10:g.28414677C>A , CM000670.1:g.28414677C>A	GRCh37
NC_000008.9:g.28470596C>A	NCBI36
NG_029723.1:g.67956C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240093.8:c.1787+1189C>A MANE Select	ENSP00000240093.3:n.1787+1189C>A
ENST00000240093.7:c.1787+1189C>A	ENSP00000240093.3:n.1787+1189C>A
ENST00000537916.2:c.1787+1189C>A	ENSP00000437489.1:n.1787+1189C>A
NM_017412.3:c.1787+1189C>A	NP_059108.1:n.1787+1189C>A
NM_145866.1:c.1787+1189C>A	NP_665873.1:n.1787+1189C>A
XM_011544646.1:c.1670+1189C>A	XP_011542948.1:n.1670+1189C>A
XM_011544647.1:c.1586+1189C>A	XP_011542949.1:n.1586+1189C>A
XM_011544649.1:c.1586+1189C>A	XP_011542951.1:n.1586+1189C>A
XR_949476.1:n.2358+1189C>A
XM_017013841.1:c.1586+1189C>A	XP_016869330.1:n.1586+1189C>A
XR_001745597.2:n.2369+1189C>A
XR_949476.2:n.2358+1189C>A
NM_017412.4:c.1787+1189C>A MANE Select	NP_059108.1:n.1787+1189C>A
NM_145866.2:c.1787+1189C>A	NP_665873.1:n.1787+1189C>A