Canonical Allele Identifier: CA1139991919
Community Standard Title: NC_000001.11:g.196651787C=
Gene: CFH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196651787C= , CM000663.2:g.196651787C= GRCh38
NC_000001.10:g.196620917C= , CM000663.1:g.196620917C= GRCh37
NC_000001.9:g.194887540C= NCBI36
NG_007259.1:g.4777C= , LRG_47:g.4777C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359637.3:c.-331C= ENSP00000352658.2:n.-331C=