Canonical Allele Identifier: CA993073481

Gene: C3

Linked Data

• dbSNP Id: rs1967870040
• gnomAD v3: 19-6710004-AGG-A
• gnomAD v4: 19-6710004-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710006_6710007del , CM000681.2:g.6710006_6710007del	GRCh38
NC_000019.9:g.6710017_6710018del , CM000681.1:g.6710017_6710018del	GRCh37
NC_000019.8:g.6661017_6661018del	NCBI36
NG_009557.1:g.15646_15647del , LRG_27:g.15646_15647del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-164_1564-163del	ENSP00000512083.1:n.1564-164_1564-163del
ENST00000695654.1:c.811-164_811-163del	ENSP00000512085.1:n.811-164_811-163del
ENST00000695655.1:c.592-128_592-127del	ENSP00000512086.1:n.592-128_592-127del
ENST00000695692.1:n.1051-164_1051-163del
ENST00000245907.11:c.1687-164_1687-163del MANE Select	ENSP00000245907.4:n.1687-164_1687-163del
ENST00000245907.10:c.1687-164_1687-163del	ENSP00000245907.4:n.1687-164_1687-163del
ENST00000600763.1:n.320-164_320-163del
NM_000064.3:c.1687-164_1687-163del	NP_000055.2:n.1687-164_1687-163del
NM_000064.4:c.1687-164_1687-163del MANE Select	NP_000055.2:n.1687-164_1687-163del