Canonical Allele Identifier: CA399798728
Gene: FZD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 488061
ClinVar RCV Id: RCV000577904 RCV001353073
dbSNP Id: rs1223920489
gnomAD v2: 17-42636356-G-A
MyVariant Identifiers: chr17:g.42636356G>A (hg19) chr17:g.44558988G>A (hg38)
PubMed: PMID:29276006
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44558988G>A , CM000679.2:g.44558988G>A GRCh38
NC_000017.10:g.42636356G>A , CM000679.1:g.42636356G>A GRCh37
NC_000017.9:g.39991882G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000315323.5:c.1300G>A MANE Select ENSP00000323901.3:p.Gly434Ser
ENST00000315323.4:c.1300G>A ENSP00000323901.3:p.Gly434Ser
NM_001466.3:c.1300G>A NP_001457.1:p.Gly434Ser
NM_001466.4:c.1300G>A MANE Select NP_001457.1:p.Gly434Ser
Search 100 bp 5'
Search 100 bp 3'