Canonical Allele Identifier: CA993073707

Gene: C3

Linked Data

• dbSNP Id: rs1967872031
• gnomAD v3: 19-6710042-A-AGGGC
• gnomAD v4: 19-6710042-A-AGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710045_6710046insCGGG , CM000681.2:g.6710045_6710046insCGGG	GRCh38
NC_000019.9:g.6710056_6710057insCGGG , CM000681.1:g.6710056_6710057insCGGG	GRCh37
NC_000019.8:g.6661056_6661057insCGGG	NCBI36
NG_009557.1:g.15609_15610insGCCC , LRG_27:g.15609_15610insGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-201_1564-200insGCCC	ENSP00000512083.1:n.1564-201_1564-200insGCCC
ENST00000695654.1:c.811-201_811-200insGCCC	ENSP00000512085.1:n.811-201_811-200insGCCC
ENST00000695655.1:c.592-165_592-164insGCCC	ENSP00000512086.1:n.592-165_592-164insGCCC
ENST00000695692.1:n.1051-201_1051-200insGCCC
ENST00000245907.11:c.1687-201_1687-200insGCCC MANE Select	ENSP00000245907.4:n.1687-201_1687-200insGCCC
ENST00000245907.10:c.1687-201_1687-200insGCCC	ENSP00000245907.4:n.1687-201_1687-200insGCCC
ENST00000600763.1:n.320-201_320-200insGCCC
NM_000064.3:c.1687-201_1687-200insGCCC	NP_000055.2:n.1687-201_1687-200insGCCC
NM_000064.4:c.1687-201_1687-200insGCCC MANE Select	NP_000055.2:n.1687-201_1687-200insGCCC