Canonical Allele Identifier: CA2320550631

Gene: C3

Linked Data

• dbSNP Id: rs1917815311

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679884A>C , CM000681.2:g.6679884A>C	GRCh38
NC_000019.9:g.6679895A>C , CM000681.1:g.6679895A>C	GRCh37
NC_000019.8:g.6630895A>C	NCBI36
NG_009557.1:g.45768T>G , LRG_27:g.45768T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2804+274T>G
ENST00000695653.1:c.2365+274T>G	ENSP00000512084.1:n.2365+274T>G
ENST00000695654.1:c.3481+274T>G	ENSP00000512085.1:n.3481+274T>G
ENST00000695689.1:c.427+274T>G	ENSP00000512101.1:n.427+274T>G
ENST00000695690.1:n.1521+274T>G
ENST00000695691.1:n.1317+274T>G
ENST00000245907.11:c.4456+274T>G MANE Select	ENSP00000245907.4:n.4456+274T>G
ENST00000245907.10:c.4456+274T>G	ENSP00000245907.4:n.4456+274T>G
ENST00000599668.1:n.51+217T>G
ENST00000599899.5:n.1415+274T>G
ENST00000601008.1:c.242-1926T>G	ENSP00000471384.1:n.242-1926T>G
NM_000064.3:c.4456+274T>G	NP_000055.2:n.4456+274T>G
NM_000064.4:c.4456+274T>G MANE Select	NP_000055.2:n.4456+274T>G