Canonical Allele Identifier: CA157153073
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs1009912860
MyVariant Identifiers: chr7:g.37991659C>T (hg19) chr7:g.37952057C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952057C>T , CM000669.2:g.37952057C>T GRCh38
NC_000007.13:g.37991659C>T , CM000669.1:g.37991659C>T GRCh37
NC_000007.12:g.37958184C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000447200.2:c.-52-25283G>A ENSP00000402262.2:n.-52-25283G>A
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