Canonical Allele Identifier: CA2320568441

Gene: C3

Linked Data

• dbSNP Id: rs1967982870

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714143C>A , CM000681.2:g.6714143C>A	GRCh38
NC_000019.9:g.6714154C>A , CM000681.1:g.6714154C>A	GRCh37
NC_000019.8:g.6665154C>A	NCBI36
NG_009557.1:g.11509G>T , LRG_27:g.11509G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.559+23G>T	ENSP00000512083.1:n.559+23G>T
ENST00000245907.11:c.682+23G>T MANE Select	ENSP00000245907.4:n.682+23G>T
ENST00000245907.10:c.682+23G>T	ENSP00000245907.4:n.682+23G>T
ENST00000595577.1:n.186+23G>T
NM_000064.3:c.682+23G>T	NP_000055.2:n.682+23G>T
NM_000064.4:c.682+23G>T MANE Select	NP_000055.2:n.682+23G>T