Canonical Allele Identifier: CA2320571979
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6720961C= , CM000681.2:g.6720961C= GRCh38
NC_000019.9:g.6720972C= , CM000681.1:g.6720972C= GRCh37
NC_000019.8:g.6671972C= NCBI36
NG_009557.1:g.4691G= , LRG_27:g.4691G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-49-1558G= ENSP00000472044.1:n.-49-1558G=