Canonical Allele Identifier: CA993073548

Gene: C3

Linked Data

• dbSNP Id: rs1967870501
• gnomAD v3: 19-6710014-AGGGAGAGAGGGC-A
• gnomAD v4: 19-6710014-AGGGAGAGAGGGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710024_6710035del , CM000681.2:g.6710024_6710035del	GRCh38
NC_000019.9:g.6710035_6710046del , CM000681.1:g.6710035_6710046del	GRCh37
NC_000019.8:g.6661035_6661046del	NCBI36
NG_009557.1:g.15626_15637del , LRG_27:g.15626_15637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-184_1564-173del	ENSP00000512083.1:n.1564-184_1564-173del
ENST00000695654.1:c.811-184_811-173del	ENSP00000512085.1:n.811-184_811-173del
ENST00000695655.1:c.592-148_592-137del	ENSP00000512086.1:n.592-148_592-137del
ENST00000695692.1:n.1051-184_1051-173del
ENST00000245907.11:c.1687-184_1687-173del MANE Select	ENSP00000245907.4:n.1687-184_1687-173del
ENST00000245907.10:c.1687-184_1687-173del	ENSP00000245907.4:n.1687-184_1687-173del
ENST00000600763.1:n.320-184_320-173del
NM_000064.3:c.1687-184_1687-173del	NP_000055.2:n.1687-184_1687-173del
NM_000064.4:c.1687-184_1687-173del MANE Select	NP_000055.2:n.1687-184_1687-173del