Canonical Allele Identifier: CA2587873191

Gene: C3

Linked Data

• gnomAD v4: 19-6684949-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684950dup , CM000681.2:g.6684950dup	GRCh38
NC_000019.9:g.6684961dup , CM000681.1:g.6684961dup	GRCh37
NC_000019.8:g.6635961dup	NCBI36
NG_009557.1:g.40702dup , LRG_27:g.40702dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2317+38dup
ENST00000695653.1:c.1878+38dup	ENSP00000512084.1:n.1878+38dup
ENST00000695654.1:c.2994+38dup	ENSP00000512085.1:n.2994+38dup
ENST00000695690.1:n.160+38dup
ENST00000695691.1:n.160+38dup
ENST00000245907.11:c.3969+38dup MANE Select	ENSP00000245907.4:n.3969+38dup
ENST00000245907.10:c.3969+38dup	ENSP00000245907.4:n.3969+38dup
ENST00000596238.1:n.412+38dup
ENST00000596548.1:c.51+38dup	ENSP00000469744.1:n.51+38dup
ENST00000601008.1:c.241+1796dup	ENSP00000471384.1:n.241+1796dup
NM_000064.3:c.3969+38dup	NP_000055.2:n.3969+38dup
NM_000064.4:c.3969+38dup MANE Select	NP_000055.2:n.3969+38dup