Canonical Allele Identifier: CA2320572859
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722611A= , CM000681.2:g.6722611A= GRCh38
NC_000019.9:g.6722622A= , CM000681.1:g.6722622A= GRCh37
NC_000019.8:g.6673622A= NCBI36
NG_009557.1:g.3041T= , LRG_27:g.3041T=

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+830T= ENSP00000472044.1:n.-50+830T=