Canonical Allele Identifier: CA1100339004
Gene: SFRP4 HGNC NCBI

Linked Data

dbSNP Id: rs1786421403
gnomAD v3: 7-37952203-C-T
gnomAD v4: 7-37952203-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37952203C>T , CM000669.2:g.37952203C>T GRCh38
NC_000007.13:g.37991805C>T , CM000669.1:g.37991805C>T GRCh37
NC_000007.12:g.37958330C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000447200.2:c.-52-25429G>A ENSP00000402262.2:n.-52-25429G>A