Canonical Allele Identifier: CA2735579584

Gene: C3

Linked Data

• dbSNP Id: rs2145425942

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709843_6709844insGAGCCCACGCAGGAGTCCT , CM000681.2:g.6709843_6709844insGAGCCCACGCAGGAGTCCT	GRCh38
NC_000019.9:g.6709854_6709855insGAGCCCACGCAGGAGTCCT , CM000681.1:g.6709854_6709855insGAGCCCACGCAGGAGTCCT	GRCh37
NC_000019.8:g.6660854_6660855insGAGCCCACGCAGGAGTCCT	NCBI36
NG_009557.1:g.15808_15809insAGGACTCCTGCGTGGGCTC , LRG_27:g.15808_15809insAGGACTCCTGCGTGGGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-2_1564-1insAGGACTCCTGCGTGGGCTC	ENSP00000512083.1:n.1564-2_1564-1insAGGACTCCTGCGTGGGCTC
ENST00000695654.1:c.811-2_811-1insAGGACTCCTGCGTGGGCTC	ENSP00000512085.1:n.811-2_811-1insAGGACTCCTGCGTGGGCTC
ENST00000695655.1:c.626_627insAGGACTCCTGCGTGGGCTC	ENSP00000512086.1:n.626_627insAGGACTCCTGCGTGGGCTC
ENST00000695692.1:n.1051-2_1051-1insAGGACTCCTGCGTGGGCTC
ENST00000245907.11:c.1687-2_1687-1insAGGACTCCTGCGTGGGCTC MANE Select	ENSP00000245907.4:n.1687-2_1687-1insAGGACTCCTGCGTGGGCTC
ENST00000245907.10:c.1687-2_1687-1insAGGACTCCTGCGTGGGCTC	ENSP00000245907.4:n.1687-2_1687-1insAGGACTCCTGCGTGGGCTC
ENST00000600763.1:n.320-2_320-1insAGGACTCCTGCGTGGGCTC
NM_000064.3:c.1687-2_1687-1insAGGACTCCTGCGTGGGCTC	NP_000055.2:n.1687-2_1687-1insAGGACTCCTGCGTGGGCTC
NM_000064.4:c.1687-2_1687-1insAGGACTCCTGCGTGGGCTC MANE Select	NP_000055.2:n.1687-2_1687-1insAGGACTCCTGCGTGGGCTC