Canonical Allele Identifier: CA2587872241

Gene: C3

Linked Data

• gnomAD v4: 19-6681885-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681885A>T , CM000681.2:g.6681885A>T	GRCh38
NC_000019.9:g.6681896A>T , CM000681.1:g.6681896A>T	GRCh37
NC_000019.8:g.6632896A>T	NCBI36
NG_009557.1:g.43767T>A , LRG_27:g.43767T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2698+56T>A
ENST00000695653.1:c.2259+56T>A	ENSP00000512084.1:n.2259+56T>A
ENST00000695654.1:c.3375+56T>A	ENSP00000512085.1:n.3375+56T>A
ENST00000695689.1:c.321+56T>A	ENSP00000512101.1:n.321+56T>A
ENST00000695690.1:n.597T>A
ENST00000695691.1:n.597T>A
ENST00000245907.11:c.4350+56T>A MANE Select	ENSP00000245907.4:n.4350+56T>A
ENST00000245907.10:c.4350+56T>A	ENSP00000245907.4:n.4350+56T>A
ENST00000596548.1:c.471+56T>A	ENSP00000469744.1:n.471+56T>A
ENST00000599899.5:n.1309+56T>A
ENST00000601008.1:c.242-3927T>A	ENSP00000471384.1:n.242-3927T>A
NM_000064.3:c.4350+56T>A	NP_000055.2:n.4350+56T>A
NM_000064.4:c.4350+56T>A MANE Select	NP_000055.2:n.4350+56T>A