Canonical Allele Identifier: CA2320572805
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722542T= , CM000681.2:g.6722542T= GRCh38
NC_000019.9:g.6722553T= , CM000681.1:g.6722553T= GRCh37
NC_000019.8:g.6673553T= NCBI36
NG_009557.1:g.3110A= , LRG_27:g.3110A=

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+899A= ENSP00000472044.1:n.-50+899A=