Canonical Allele Identifier: CA382018213
Gene: FZD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1430811
ClinVar RCV Id: RCV001931585
dbSNP Id: rs759980701

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86954845T>A , CM000673.2:g.86954845T>A GRCh38
NC_000011.9:g.86665887T>A , CM000673.1:g.86665887T>A GRCh37
NC_000011.8:g.86343535T>A NCBI36
NG_011752.1:g.5547A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.241A>T MANE Select ENSP00000434034.1:p.Thr81Ser
ENST00000531380.1:c.241A>T ENSP00000434034.1:p.Thr81Ser
NM_012193.3:c.241A>T NP_036325.2:p.Thr81Ser
NM_012193.4:c.241A>T MANE Select NP_036325.2:p.Thr81Ser