Canonical Allele Identifier: CA2587875491

Gene: C3

Linked Data

• gnomAD v4: 19-6697911-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697911T>A , CM000681.2:g.6697911T>A	GRCh38
NC_000019.9:g.6697922T>A , CM000681.1:g.6697922T>A	GRCh37
NC_000019.8:g.6648922T>A	NCBI36
NG_009557.1:g.27741A>T , LRG_27:g.27741A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-117A>T
ENST00000695652.1:c.2318-117A>T	ENSP00000512083.1:n.2318-117A>T
ENST00000695653.1:c.350-117A>T	ENSP00000512084.1:n.350-117A>T
ENST00000695654.1:c.1565-117A>T	ENSP00000512085.1:n.1565-117A>T
ENST00000695655.1:c.1382-117A>T	ENSP00000512086.1:n.1382-117A>T
ENST00000695692.1:n.1805-117A>T
ENST00000245907.11:c.2441-117A>T MANE Select	ENSP00000245907.4:n.2441-117A>T
ENST00000245907.10:c.2441-117A>T	ENSP00000245907.4:n.2441-117A>T
ENST00000602053.1:n.489-117A>T
NM_000064.3:c.2441-117A>T	NP_000055.2:n.2441-117A>T
NM_000064.4:c.2441-117A>T MANE Select	NP_000055.2:n.2441-117A>T