Canonical Allele Identifier: CA1700849002
Gene: SFRP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.38021183T= , CM000669.2:g.38021183T= GRCh38
NC_000007.13:g.38060785T= , CM000669.1:g.38060785T= GRCh37
NC_000007.12:g.38027310T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000447200.2:c.-53+4127A= ENSP00000402262.2:n.-53+4127A=
XR_001745170.1:n.832+7602T=
XR_927181.1:n.576+7602T=