Canonical Allele Identifier: CA631722461

Gene: C3

Linked Data

• gnomAD v2: 19-6710019-A-AGAGAGAGGGAGAGAGGGAGG
• gnomAD v3: 19-6710008-A-AGAGAGAGGGAGAGAGGGAGG
• gnomAD v4: 19-6710008-A-AGAGAGAGGGAGAGAGGGAGG
• MyVariant Identifiers: chr19:g.6710019_6710020insGAGAGAGGGAGAGAGGGAGG (hg19) ; chr19:g.6710008_6710009insGAGAGAGGGAGAGAGGGAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGGGAGAGAGGG , CM000681.2:g.6710025_6710026insAGGGAGAGAGGGAGAGAGGG	GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGGGAGAGAGGG , CM000681.1:g.6710036_6710037insAGGGAGAGAGGGAGAGAGGG	GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGGGAGAGAGGG	NCBI36
NG_009557.1:g.15643_15644insCCTCCCTCTCTCCCTCTCTC , LRG_27:g.15643_15644insCCTCCCTCTCTCCCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-167_1564-166insCCTCCCTCTCTCCCTCTCTC	ENSP00000512083.1:n.1564-167_1564-166insCCTCCCTCTCTCCCTCTCTC
ENST00000695654.1:c.811-167_811-166insCCTCCCTCTCTCCCTCTCTC	ENSP00000512085.1:n.811-167_811-166insCCTCCCTCTCTCCCTCTCTC
ENST00000695655.1:c.592-131_592-130insCCTCCCTCTCTCCCTCTCTC	ENSP00000512086.1:n.592-131_592-130insCCTCCCTCTCTCCCTCTCTC
ENST00000695692.1:n.1051-167_1051-166insCCTCCCTCTCTCCCTCTCTC
ENST00000245907.11:c.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC MANE Select	ENSP00000245907.4:n.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC
ENST00000245907.10:c.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC	ENSP00000245907.4:n.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC
ENST00000600763.1:n.320-167_320-166insCCTCCCTCTCTCCCTCTCTC
NM_000064.3:c.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC	NP_000055.2:n.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC
NM_000064.4:c.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC MANE Select	NP_000055.2:n.1687-167_1687-166insCCTCCCTCTCTCCCTCTCTC