Canonical Allele Identifier: CA838220492
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs1346016935
MyVariant Identifiers: chr7:g.37991826C>T (hg19) chr7:g.37952224C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952224C>T , CM000669.2:g.37952224C>T GRCh38
NC_000007.13:g.37991826C>T , CM000669.1:g.37991826C>T GRCh37
NC_000007.12:g.37958351C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000447200.2:c.-52-25450G>A ENSP00000402262.2:n.-52-25450G>A
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