Canonical Allele Identifier: CA1700819861
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs1786420025

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952135A>G , CM000669.2:g.37952135A>G GRCh38
NC_000007.13:g.37991737A>G , CM000669.1:g.37991737A>G GRCh37
NC_000007.12:g.37958262A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000447200.2:c.-52-25361T>C ENSP00000402262.2:n.-52-25361T>C