Canonical Allele Identifier: CA2587875422

Gene: C3

Linked Data

• gnomAD v4: 19-6697831-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697835dup , CM000681.2:g.6697835dup	GRCh38
NC_000019.9:g.6697846dup , CM000681.1:g.6697846dup	GRCh37
NC_000019.8:g.6648846dup	NCBI36
NG_009557.1:g.27820dup , LRG_27:g.27820dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-38dup
ENST00000695652.1:c.2318-38dup	ENSP00000512083.1:n.2318-38dup
ENST00000695653.1:c.350-38dup	ENSP00000512084.1:n.350-38dup
ENST00000695654.1:c.1565-38dup	ENSP00000512085.1:n.1565-38dup
ENST00000695655.1:c.1382-38dup	ENSP00000512086.1:n.1382-38dup
ENST00000695692.1:n.1805-38dup
ENST00000245907.11:c.2441-38dup MANE Select	ENSP00000245907.4:n.2441-38dup
ENST00000245907.10:c.2441-38dup	ENSP00000245907.4:n.2441-38dup
ENST00000602053.1:n.489-38dup
NM_000064.3:c.2441-38dup	NP_000055.2:n.2441-38dup
NM_000064.4:c.2441-38dup MANE Select	NP_000055.2:n.2441-38dup