Canonical Allele Identifier: CA2320568603

Gene: C3

Linked Data

• dbSNP Id: rs1967990887
• gnomAD v4: 19-6714501-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714502_6714503dup , CM000681.2:g.6714502_6714503dup	GRCh38
NC_000019.9:g.6714513_6714514dup , CM000681.1:g.6714513_6714514dup	GRCh37
NC_000019.8:g.6665513_6665514dup	NCBI36
NG_009557.1:g.11149_11150dup , LRG_27:g.11149_11150dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.382-57_382-56dup	ENSP00000512083.1:n.382-57_382-56dup
ENST00000245907.11:c.505-57_505-56dup MANE Select	ENSP00000245907.4:n.505-57_505-56dup
ENST00000245907.10:c.505-57_505-56dup	ENSP00000245907.4:n.505-57_505-56dup
NM_000064.3:c.505-57_505-56dup	NP_000055.2:n.505-57_505-56dup
NM_000064.4:c.505-57_505-56dup MANE Select	NP_000055.2:n.505-57_505-56dup