Canonical Allele Identifier: CA157153123
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs532533027
gnomAD v2: 7-37991755-A-G
gnomAD v3: 7-37952153-A-G
gnomAD v4: 7-37952153-A-G
MyVariant Identifiers: chr7:g.37991755A>G (hg19) chr7:g.37952153A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952153A>G , CM000669.2:g.37952153A>G GRCh38
NC_000007.13:g.37991755A>G , CM000669.1:g.37991755A>G GRCh37
NC_000007.12:g.37958280A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000447200.2:c.-52-25379T>C ENSP00000402262.2:n.-52-25379T>C
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