Canonical Allele Identifier: CA2320572803
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1968205873

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722541A>G , CM000681.2:g.6722541A>G GRCh38
NC_000019.9:g.6722552A>G , CM000681.1:g.6722552A>G GRCh37
NC_000019.8:g.6673552A>G NCBI36
NG_009557.1:g.3111T>C , LRG_27:g.3111T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+900T>C ENSP00000472044.1:n.-50+900T>C