Canonical Allele Identifier: CA2320559334

Gene: C3

Linked Data

• dbSNP Id: rs1967576395

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698004_6698005del , CM000681.2:g.6698004_6698005del	GRCh38
NC_000019.9:g.6698015_6698016del , CM000681.1:g.6698015_6698016del	GRCh37
NC_000019.8:g.6649015_6649016del	NCBI36
NG_009557.1:g.27648_27649del , LRG_27:g.27648_27649del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-210_789-209del
ENST00000695652.1:c.2318-210_2318-209del	ENSP00000512083.1:n.2318-210_2318-209del
ENST00000695653.1:c.350-210_350-209del	ENSP00000512084.1:n.350-210_350-209del
ENST00000695654.1:c.1565-210_1565-209del	ENSP00000512085.1:n.1565-210_1565-209del
ENST00000695655.1:c.1382-210_1382-209del	ENSP00000512086.1:n.1382-210_1382-209del
ENST00000695692.1:n.1805-210_1805-209del
ENST00000245907.11:c.2441-210_2441-209del MANE Select	ENSP00000245907.4:n.2441-210_2441-209del
ENST00000245907.10:c.2441-210_2441-209del	ENSP00000245907.4:n.2441-210_2441-209del
ENST00000602053.1:n.489-210_489-209del
NM_000064.3:c.2441-210_2441-209del	NP_000055.2:n.2441-210_2441-209del
NM_000064.4:c.2441-210_2441-209del MANE Select	NP_000055.2:n.2441-210_2441-209del