Canonical Allele Identifier: CA2320572857
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722610A= , CM000681.2:g.6722610A= GRCh38
NC_000019.9:g.6722621A= , CM000681.1:g.6722621A= GRCh37
NC_000019.8:g.6673621A= NCBI36
NG_009557.1:g.3042T= , LRG_27:g.3042T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-50+831T= ENSP00000472044.1:n.-50+831T=