Canonical Allele Identifier: CA2320567687

Gene: C3

Linked Data

• dbSNP Id: rs1967948925

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712857dup , CM000681.2:g.6712857dup	GRCh38
NC_000019.9:g.6712868dup , CM000681.1:g.6712868dup	GRCh37
NC_000019.8:g.6663868dup	NCBI36
NG_009557.1:g.12798dup , LRG_27:g.12798dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-231dup	ENSP00000512083.1:n.881-231dup
ENST00000695654.1:c.128-231dup	ENSP00000512085.1:n.128-231dup
ENST00000695692.1:n.328-191dup
ENST00000245907.11:c.1004-231dup MANE Select	ENSP00000245907.4:n.1004-231dup
ENST00000245907.10:c.1004-231dup	ENSP00000245907.4:n.1004-231dup
ENST00000594270.5:n.128-252dup
ENST00000595577.1:n.508-231dup
ENST00000597442.5:n.254-231dup
NM_000064.3:c.1004-231dup	NP_000055.2:n.1004-231dup
NM_000064.4:c.1004-231dup MANE Select	NP_000055.2:n.1004-231dup