Canonical Allele Identifier: CA174665184

Gene: FZD3

Linked Data

• dbSNP Id: rs376793949
• MyVariant Identifiers: chr8:g.28390886C>G (hg19) ; chr8:g.28533369C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28533369C>G , CM000670.2:g.28533369C>G	GRCh38
NC_000008.10:g.28390886C>G , CM000670.1:g.28390886C>G	GRCh37
NC_000008.9:g.28446805C>G	NCBI36
NG_029723.1:g.44165C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000240093.8:c.1404+5205C>G MANE Select	ENSP00000240093.3:n.1404+5205C>G
ENST00000240093.7:c.1404+5205C>G	ENSP00000240093.3:n.1404+5205C>G
ENST00000537916.2:c.1404+5205C>G	ENSP00000437489.1:n.1404+5205C>G
NM_017412.3:c.1404+5205C>G	NP_059108.1:n.1404+5205C>G
NM_145866.1:c.1404+5205C>G	NP_665873.1:n.1404+5205C>G
XM_011544646.1:c.1287+5205C>G	XP_011542948.1:n.1287+5205C>G
XM_011544647.1:c.1203+5205C>G	XP_011542949.1:n.1203+5205C>G
XM_011544649.1:c.1203+5205C>G	XP_011542951.1:n.1203+5205C>G
XR_949476.1:n.1924-3524C>G
XR_949477.1:n.1924-3524C>G
XR_949478.1:n.1923+5205C>G
XM_017013841.1:c.1203+5205C>G	XP_016869330.1:n.1203+5205C>G
XM_017013842.1:c.1405-3524C>G	XP_016869331.1:n.1405-3524C>G
XM_017013843.1:c.1405-3524C>G	XP_016869332.1:n.1405-3524C>G
XM_017013844.1:c.1404+5205C>G	XP_016869333.1:n.1404+5205C>G
XR_001745597.2:n.1880+5205C>G
XR_949476.2:n.1924-3524C>G
NM_017412.4:c.1404+5205C>G MANE Select	NP_059108.1:n.1404+5205C>G
NM_145866.2:c.1404+5205C>G	NP_665873.1:n.1404+5205C>G