Canonical Allele Identifier: CA2320572808
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1968206263

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722556del , CM000681.2:g.6722556del GRCh38
NC_000019.9:g.6722567del , CM000681.1:g.6722567del GRCh37
NC_000019.8:g.6673567del NCBI36
NG_009557.1:g.3098del , LRG_27:g.3098del

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+887del ENSP00000472044.1:n.-50+887del