Canonical Allele Identifier: CA2587878451

Gene: C3

Linked Data

• gnomAD v4: 19-6713657-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713662del , CM000681.2:g.6713662del	GRCh38
NC_000019.9:g.6713673del , CM000681.1:g.6713673del	GRCh37
NC_000019.8:g.6664673del	NCBI36
NG_009557.1:g.11994del , LRG_27:g.11994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-149del	ENSP00000512083.1:n.651-149del
ENST00000245907.11:c.774-149del MANE Select	ENSP00000245907.4:n.774-149del
ENST00000245907.10:c.774-149del	ENSP00000245907.4:n.774-149del
ENST00000595577.1:n.278-149del
ENST00000597442.5:n.23+108del
NM_000064.3:c.774-149del	NP_000055.2:n.774-149del
NM_000064.4:c.774-149del MANE Select	NP_000055.2:n.774-149del