Canonical Allele Identifier: CA1100338995
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs1786420552
gnomAD v3: 7-37952162-G-C
gnomAD v4: 7-37952162-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952162G>C , CM000669.2:g.37952162G>C GRCh38
NC_000007.13:g.37991764G>C , CM000669.1:g.37991764G>C GRCh37
NC_000007.12:g.37958289G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000447200.2:c.-52-25388C>G ENSP00000402262.2:n.-52-25388C>G
Search 100 bp 5'
Search 100 bp 3'