Canonical Allele Identifier: CA573962359
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs1242810448
gnomAD v2: 7-37991785-C-A
gnomAD v3: 7-37952183-C-A
gnomAD v4: 7-37952183-C-A
MyVariant Identifiers: chr7:g.37991785C>A (hg19) chr7:g.37952183C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952183C>A , CM000669.2:g.37952183C>A GRCh38
NC_000007.13:g.37991785C>A , CM000669.1:g.37991785C>A GRCh37
NC_000007.12:g.37958310C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000447200.2:c.-52-25409G>T ENSP00000402262.2:n.-52-25409G>T
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