Canonical Allele Identifier: CA2320572934
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722727C= , CM000681.2:g.6722727C= GRCh38
NC_000019.9:g.6722738C= , CM000681.1:g.6722738C= GRCh37
NC_000019.8:g.6673738C= NCBI36
NG_009557.1:g.2925G= , LRG_27:g.2925G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-50+714G= ENSP00000472044.1:n.-50+714G=