Canonical Allele Identifier: CA1112202628

Gene: FZD3

Linked Data

• dbSNP Id: rs1804931110
• gnomAD v3: 8-28533464-T-C
• gnomAD v4: 8-28533464-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28533464T>C , CM000670.2:g.28533464T>C	GRCh38
NC_000008.10:g.28390981T>C , CM000670.1:g.28390981T>C	GRCh37
NC_000008.9:g.28446900T>C	NCBI36
NG_029723.1:g.44260T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000240093.8:c.1404+5300T>C MANE Select	ENSP00000240093.3:n.1404+5300T>C
ENST00000240093.7:c.1404+5300T>C	ENSP00000240093.3:n.1404+5300T>C
ENST00000537916.2:c.1404+5300T>C	ENSP00000437489.1:n.1404+5300T>C
NM_017412.3:c.1404+5300T>C	NP_059108.1:n.1404+5300T>C
NM_145866.1:c.1404+5300T>C	NP_665873.1:n.1404+5300T>C
XM_011544646.1:c.1287+5300T>C	XP_011542948.1:n.1287+5300T>C
XM_011544647.1:c.1203+5300T>C	XP_011542949.1:n.1203+5300T>C
XM_011544649.1:c.1203+5300T>C	XP_011542951.1:n.1203+5300T>C
XR_949476.1:n.1924-3429T>C
XR_949477.1:n.1924-3429T>C
XR_949478.1:n.1923+5300T>C
XM_017013841.1:c.1203+5300T>C	XP_016869330.1:n.1203+5300T>C
XM_017013842.1:c.1405-3429T>C	XP_016869331.1:n.1405-3429T>C
XM_017013843.1:c.1405-3429T>C	XP_016869332.1:n.1405-3429T>C
XM_017013844.1:c.1404+5300T>C	XP_016869333.1:n.1404+5300T>C
XR_001745597.2:n.1880+5300T>C
XR_949476.2:n.1924-3429T>C
NM_017412.4:c.1404+5300T>C MANE Select	NP_059108.1:n.1404+5300T>C
NM_145866.2:c.1404+5300T>C	NP_665873.1:n.1404+5300T>C