Canonical Allele Identifier: CA2320559329

Gene: C3

Linked Data

• dbSNP Id: rs1967576005

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698001_6698002del , CM000681.2:g.6698001_6698002del	GRCh38
NC_000019.9:g.6698012_6698013del , CM000681.1:g.6698012_6698013del	GRCh37
NC_000019.8:g.6649012_6649013del	NCBI36
NG_009557.1:g.27651_27652del , LRG_27:g.27651_27652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-207_789-206del
ENST00000695652.1:c.2318-207_2318-206del	ENSP00000512083.1:n.2318-207_2318-206del
ENST00000695653.1:c.350-207_350-206del	ENSP00000512084.1:n.350-207_350-206del
ENST00000695654.1:c.1565-207_1565-206del	ENSP00000512085.1:n.1565-207_1565-206del
ENST00000695655.1:c.1382-207_1382-206del	ENSP00000512086.1:n.1382-207_1382-206del
ENST00000695692.1:n.1805-207_1805-206del
ENST00000245907.11:c.2441-207_2441-206del MANE Select	ENSP00000245907.4:n.2441-207_2441-206del
ENST00000245907.10:c.2441-207_2441-206del	ENSP00000245907.4:n.2441-207_2441-206del
ENST00000602053.1:n.489-207_489-206del
NM_000064.3:c.2441-207_2441-206del	NP_000055.2:n.2441-207_2441-206del
NM_000064.4:c.2441-207_2441-206del MANE Select	NP_000055.2:n.2441-207_2441-206del