Canonical Allele Identifier: CA1700819872
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs1786420207

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952143C>G , CM000669.2:g.37952143C>G GRCh38
NC_000007.13:g.37991745C>G , CM000669.1:g.37991745C>G GRCh37
NC_000007.12:g.37958270C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000447200.2:c.-52-25369G>C ENSP00000402262.2:n.-52-25369G>C