Canonical Allele Identifier: CA993073300

Gene: C3

Linked Data

• dbSNP Id: rs1967868958
• gnomAD v3: 19-6709975-GAGGGAGAGAGAGAGAA-G
• gnomAD v4: 19-6709975-GAGGGAGAGAGAGAGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709986_6710001del , CM000681.2:g.6709986_6710001del	GRCh38
NC_000019.9:g.6709997_6710012del , CM000681.1:g.6709997_6710012del	GRCh37
NC_000019.8:g.6660997_6661012del	NCBI36
NG_009557.1:g.15661_15676del , LRG_27:g.15661_15676del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-149_1564-134del	ENSP00000512083.1:n.1564-149_1564-134del
ENST00000695654.1:c.811-149_811-134del	ENSP00000512085.1:n.811-149_811-134del
ENST00000695655.1:c.592-113_592-98del	ENSP00000512086.1:n.592-113_592-98del
ENST00000695692.1:n.1051-149_1051-134del
ENST00000245907.11:c.1687-149_1687-134del MANE Select	ENSP00000245907.4:n.1687-149_1687-134del
ENST00000245907.10:c.1687-149_1687-134del	ENSP00000245907.4:n.1687-149_1687-134del
ENST00000600763.1:n.320-149_320-134del
NM_000064.3:c.1687-149_1687-134del	NP_000055.2:n.1687-149_1687-134del
NM_000064.4:c.1687-149_1687-134del MANE Select	NP_000055.2:n.1687-149_1687-134del