Canonical Allele Identifier: CA631722456

Gene: C3

Linked Data

• dbSNP Id: rs1967869542
• gnomAD v2: 19-6710002-A-AAGGGAGAGAGGGAGGGAAAGAG
• gnomAD v3: 19-6709991-A-AAGGGAGAGAGGGAGGGAAAGAG
• gnomAD v4: 19-6709991-A-AAGGGAGAGAGGGAGGGAAAGAG
• MyVariant Identifiers: chr19:g.6710002_6710003insAGGGAGAGAGGGAGGGAAAGAG (hg19) ; chr19:g.6709991_6709992insAGGGAGAGAGGGAGGGAAAGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710008_6710009insAAGAGAGGGAGAGAGGGAGGGA , CM000681.2:g.6710008_6710009insAAGAGAGGGAGAGAGGGAGGGA	GRCh38
NC_000019.9:g.6710019_6710020insAAGAGAGGGAGAGAGGGAGGGA , CM000681.1:g.6710019_6710020insAAGAGAGGGAGAGAGGGAGGGA	GRCh37
NC_000019.8:g.6661019_6661020insAAGAGAGGGAGAGAGGGAGGGA	NCBI36
NG_009557.1:g.15660_15661insCTCTTTCCCTCCCTCTCTCCCT , LRG_27:g.15660_15661insCTCTTTCCCTCCCTCTCTCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-150_1564-149insCTCTTTCCCTCCCTCTCTCCCT	ENSP00000512083.1:n.1564-150_1564-149insCTCTTTCCCTCCCTCTCTCCC...
ENST00000695654.1:c.811-150_811-149insCTCTTTCCCTCCCTCTCTCCCT	ENSP00000512085.1:n.811-150_811-149insCTCTTTCCCTCCCTCTCTCCCT
ENST00000695655.1:c.592-114_592-113insCTCTTTCCCTCCCTCTCTCCCT	ENSP00000512086.1:n.592-114_592-113insCTCTTTCCCTCCCTCTCTCCCT
ENST00000695692.1:n.1051-150_1051-149insCTCTTTCCCTCCCTCTCTCCCT
ENST00000245907.11:c.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCCT MANE Select	ENSP00000245907.4:n.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCC...
ENST00000245907.10:c.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCCT	ENSP00000245907.4:n.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCC...
ENST00000600763.1:n.320-150_320-149insCTCTTTCCCTCCCTCTCTCCCT
NM_000064.3:c.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCCT	NP_000055.2:n.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCCT
NM_000064.4:c.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCCT MANE Select	NP_000055.2:n.1687-150_1687-149insCTCTTTCCCTCCCTCTCTCCCT