Canonical Allele Identifier: CA157153132
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs760047376
MyVariant Identifiers: chr7:g.37991814C>A (hg19) chr7:g.37952212C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952212C>A , CM000669.2:g.37952212C>A GRCh38
NC_000007.13:g.37991814C>A , CM000669.1:g.37991814C>A GRCh37
NC_000007.12:g.37958339C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000447200.2:c.-52-25438G>T ENSP00000402262.2:n.-52-25438G>T
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