Canonical Allele Identifier: CA631722469

Gene: C3

Linked Data

• gnomAD v2: 19-6710061-A-AGGG
• gnomAD v3: 19-6710050-A-AGGG
• gnomAD v4: 19-6710050-A-AGGG
• MyVariant Identifiers: chr19:g.6710061_6710062insGGG (hg19) ; chr19:g.6710050_6710051insGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710050_6710051insGGG , CM000681.2:g.6710050_6710051insGGG	GRCh38
NC_000019.9:g.6710061_6710062insGGG , CM000681.1:g.6710061_6710062insGGG	GRCh37
NC_000019.8:g.6661061_6661062insGGG	NCBI36
NG_009557.1:g.15601_15602insCCC , LRG_27:g.15601_15602insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-209_1564-208insCCC	ENSP00000512083.1:n.1564-209_1564-208insCCC
ENST00000695654.1:c.811-209_811-208insCCC	ENSP00000512085.1:n.811-209_811-208insCCC
ENST00000695655.1:c.592-173_592-172insCCC	ENSP00000512086.1:n.592-173_592-172insCCC
ENST00000695692.1:n.1051-209_1051-208insCCC
ENST00000245907.11:c.1687-209_1687-208insCCC MANE Select	ENSP00000245907.4:n.1687-209_1687-208insCCC
ENST00000245907.10:c.1687-209_1687-208insCCC	ENSP00000245907.4:n.1687-209_1687-208insCCC
ENST00000600763.1:n.320-209_320-208insCCC
NM_000064.3:c.1687-209_1687-208insCCC	NP_000055.2:n.1687-209_1687-208insCCC
NM_000064.4:c.1687-209_1687-208insCCC MANE Select	NP_000055.2:n.1687-209_1687-208insCCC