Canonical Allele Identifier: CA1140206447
Gene: CFHR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196883651T= , CM000663.2:g.196883651T= GRCh38
NC_000001.10:g.196852781T= , CM000663.1:g.196852781T= GRCh37
NC_000001.9:g.195119404T= NCBI36
NG_028159.1:g.638T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649395.1:n.427-955T=
ENST00000367421.4:c.58+63749T= ENSP00000356391.3:n.58+63749T=
ENST00000608469.5:c.43+25243T= ENSP00000477162.1:n.43+25243T=