Canonical Allele Identifier: CA2320550534

Gene: C3

Linked Data

• dbSNP Id: rs1917810979

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679664del , CM000681.2:g.6679664del	GRCh38
NC_000019.9:g.6679675del , CM000681.1:g.6679675del	GRCh37
NC_000019.8:g.6630675del	NCBI36
NG_009557.1:g.45988del , LRG_27:g.45988del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-168del
ENST00000695653.1:c.2366-168del	ENSP00000512084.1:n.2366-168del
ENST00000695654.1:c.3482-168del	ENSP00000512085.1:n.3482-168del
ENST00000695689.1:c.428-168del	ENSP00000512101.1:n.428-168del
ENST00000695690.1:n.1522-168del
ENST00000695691.1:n.1318-168del
ENST00000245907.11:c.4457-168del MANE Select	ENSP00000245907.4:n.4457-168del
ENST00000245907.10:c.4457-168del	ENSP00000245907.4:n.4457-168del
ENST00000599668.1:n.52-168del
ENST00000599899.5:n.1416-168del
ENST00000601008.1:c.242-1706del	ENSP00000471384.1:n.242-1706del
NM_000064.3:c.4457-168del	NP_000055.2:n.4457-168del
NM_000064.4:c.4457-168del MANE Select	NP_000055.2:n.4457-168del