Canonical Allele Identifier: CA2320553524

Gene: C3

Linked Data

• dbSNP Id: rs1918009475
• gnomAD v4: 19-6686340-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686340A>T , CM000681.2:g.6686340A>T	GRCh38
NC_000019.9:g.6686351A>T , CM000681.1:g.6686351A>T	GRCh37
NC_000019.8:g.6637351A>T	NCBI36
NG_009557.1:g.39312T>A , LRG_27:g.39312T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-53T>A
ENST00000695652.1:c.3524-53T>A	ENSP00000512083.1:n.3524-53T>A
ENST00000695653.1:c.1556-53T>A	ENSP00000512084.1:n.1556-53T>A
ENST00000695654.1:c.2672-53T>A	ENSP00000512085.1:n.2672-53T>A
ENST00000695655.1:c.2588-53T>A	ENSP00000512086.1:n.2588-53T>A
ENST00000695692.1:n.3011-53T>A
ENST00000245907.11:c.3647-53T>A MANE Select	ENSP00000245907.4:n.3647-53T>A
ENST00000245907.10:c.3647-53T>A	ENSP00000245907.4:n.3647-53T>A
ENST00000596238.1:n.37T>A
ENST00000598805.2:n.822T>A
ENST00000601008.1:c.241+406T>A	ENSP00000471384.1:n.241+406T>A
NM_000064.3:c.3647-53T>A	NP_000055.2:n.3647-53T>A
NM_000064.4:c.3647-53T>A MANE Select	NP_000055.2:n.3647-53T>A