Canonical Allele Identifier: CA257691
Gene: C3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 17060
ClinVar RCV Id: RCV000018589
dbSNP Id: rs121909583

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709754C>T , CM000681.2:g.6709754C>T GRCh38
NC_000019.9:g.6709765C>T , CM000681.1:g.6709765C>T GRCh37
NC_000019.8:g.6660765C>T NCBI36
NG_009557.1:g.15898G>A , LRG_27:g.15898G>A

Transcript Alleles

HGVS Amino-acid change
NM_000064.3:c.1775G>A VV NP_000055.2:p.Arg592Gln
ENST00000245907.10:c.1775G>A ENSP00000245907.4:p.Arg592Gln