Canonical Allele Identifier: CA174665176
Gene: FZD3 HGNC NCBI

Linked Data

dbSNP Id: rs749300001
gnomAD v2: 8-28390817-G-A
gnomAD v3: 8-28533300-G-A
gnomAD v4: 8-28533300-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28533300G>A , CM000670.2:g.28533300G>A GRCh38
NC_000008.10:g.28390817G>A , CM000670.1:g.28390817G>A GRCh37
NC_000008.9:g.28446736G>A NCBI36
NG_029723.1:g.44096G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000240093.8:c.1404+5136G>A MANE Select ENSP00000240093.3:n.1404+5136G>A
ENST00000240093.7:c.1404+5136G>A ENSP00000240093.3:n.1404+5136G>A
ENST00000537916.2:c.1404+5136G>A ENSP00000437489.1:n.1404+5136G>A
NM_017412.3:c.1404+5136G>A NP_059108.1:n.1404+5136G>A
NM_145866.1:c.1404+5136G>A NP_665873.1:n.1404+5136G>A
XM_011544646.1:c.1287+5136G>A XP_011542948.1:n.1287+5136G>A
XM_011544647.1:c.1203+5136G>A XP_011542949.1:n.1203+5136G>A
XM_011544649.1:c.1203+5136G>A XP_011542951.1:n.1203+5136G>A
XR_949476.1:n.1924-3593G>A
XR_949477.1:n.1924-3593G>A
XR_949478.1:n.1923+5136G>A
XM_017013841.1:c.1203+5136G>A XP_016869330.1:n.1203+5136G>A
XM_017013842.1:c.1405-3593G>A XP_016869331.1:n.1405-3593G>A
XM_017013843.1:c.1405-3593G>A XP_016869332.1:n.1405-3593G>A
XM_017013844.1:c.1404+5136G>A XP_016869333.1:n.1404+5136G>A
XR_001745597.2:n.1880+5136G>A
XR_949476.2:n.1924-3593G>A
NM_017412.4:c.1404+5136G>A MANE Select NP_059108.1:n.1404+5136G>A
NM_145866.2:c.1404+5136G>A NP_665873.1:n.1404+5136G>A