Canonical Allele Identifier: CA993073699

Gene: C3

Linked Data

• dbSNP Id: rs1967871914
• gnomAD v3: 19-6710040-AAAGG-A
• gnomAD v4: 19-6710040-AAAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710041_6710044del , CM000681.2:g.6710041_6710044del	GRCh38
NC_000019.9:g.6710052_6710055del , CM000681.1:g.6710052_6710055del	GRCh37
NC_000019.8:g.6661052_6661055del	NCBI36
NG_009557.1:g.15608_15611del , LRG_27:g.15608_15611del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-202_1564-199del	ENSP00000512083.1:n.1564-202_1564-199del
ENST00000695654.1:c.811-202_811-199del	ENSP00000512085.1:n.811-202_811-199del
ENST00000695655.1:c.592-166_592-163del	ENSP00000512086.1:n.592-166_592-163del
ENST00000695692.1:n.1051-202_1051-199del
ENST00000245907.11:c.1687-202_1687-199del MANE Select	ENSP00000245907.4:n.1687-202_1687-199del
ENST00000245907.10:c.1687-202_1687-199del	ENSP00000245907.4:n.1687-202_1687-199del
ENST00000600763.1:n.320-202_320-199del
NM_000064.3:c.1687-202_1687-199del	NP_000055.2:n.1687-202_1687-199del
NM_000064.4:c.1687-202_1687-199del MANE Select	NP_000055.2:n.1687-202_1687-199del