Canonical Allele Identifier: CA2320567976

Gene: C3

Linked Data

• dbSNP Id: rs1967965569

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713547_6713549del , CM000681.2:g.6713547_6713549del	GRCh38
NC_000019.9:g.6713558_6713560del , CM000681.1:g.6713558_6713560del	GRCh37
NC_000019.8:g.6664558_6664560del	NCBI36
NG_009557.1:g.12106_12108del , LRG_27:g.12106_12108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-37_651-35del	ENSP00000512083.1:n.651-37_651-35del
ENST00000695692.1:n.61_63del
ENST00000245907.11:c.774-37_774-35del MANE Select	ENSP00000245907.4:n.774-37_774-35del
ENST00000245907.10:c.774-37_774-35del	ENSP00000245907.4:n.774-37_774-35del
ENST00000595577.1:n.278-37_278-35del
ENST00000597442.5:n.24-37_24-35del
NM_000064.3:c.774-37_774-35del	NP_000055.2:n.774-37_774-35del
NM_000064.4:c.774-37_774-35del MANE Select	NP_000055.2:n.774-37_774-35del