Canonical Allele Identifier: CA174665175
Gene: FZD3 HGNC NCBI

Linked Data

dbSNP Id: rs375014519
gnomAD v2: 8-28390813-C-T
gnomAD v3: 8-28533296-C-T
gnomAD v4: 8-28533296-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28533296C>T , CM000670.2:g.28533296C>T GRCh38
NC_000008.10:g.28390813C>T , CM000670.1:g.28390813C>T GRCh37
NC_000008.9:g.28446732C>T NCBI36
NG_029723.1:g.44092C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000240093.8:c.1404+5132C>T MANE Select ENSP00000240093.3:n.1404+5132C>T
ENST00000240093.7:c.1404+5132C>T ENSP00000240093.3:n.1404+5132C>T
ENST00000537916.2:c.1404+5132C>T ENSP00000437489.1:n.1404+5132C>T
NM_017412.3:c.1404+5132C>T NP_059108.1:n.1404+5132C>T
NM_145866.1:c.1404+5132C>T NP_665873.1:n.1404+5132C>T
XM_011544646.1:c.1287+5132C>T XP_011542948.1:n.1287+5132C>T
XM_011544647.1:c.1203+5132C>T XP_011542949.1:n.1203+5132C>T
XM_011544649.1:c.1203+5132C>T XP_011542951.1:n.1203+5132C>T
XR_949476.1:n.1924-3597C>T
XR_949477.1:n.1924-3597C>T
XR_949478.1:n.1923+5132C>T
XM_017013841.1:c.1203+5132C>T XP_016869330.1:n.1203+5132C>T
XM_017013842.1:c.1405-3597C>T XP_016869331.1:n.1405-3597C>T
XM_017013843.1:c.1405-3597C>T XP_016869332.1:n.1405-3597C>T
XM_017013844.1:c.1404+5132C>T XP_016869333.1:n.1404+5132C>T
XR_001745597.2:n.1880+5132C>T
XR_949476.2:n.1924-3597C>T
NM_017412.4:c.1404+5132C>T MANE Select NP_059108.1:n.1404+5132C>T
NM_145866.2:c.1404+5132C>T NP_665873.1:n.1404+5132C>T