Canonical Allele Identifier: CA2320550339

Gene: C3

Linked Data

• dbSNP Id: rs1917796736

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679265_6679267del , CM000681.2:g.6679265_6679267del	GRCh38
NC_000019.9:g.6679276_6679278del , CM000681.1:g.6679276_6679278del	GRCh37
NC_000019.8:g.6630276_6630278del	NCBI36
NG_009557.1:g.46385_46387del , LRG_27:g.46385_46387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2895-59_2895-57del
ENST00000695653.1:c.2456-59_2456-57del	ENSP00000512084.1:n.2456-59_2456-57del
ENST00000695654.1:c.3572-59_3572-57del	ENSP00000512085.1:n.3572-59_3572-57del
ENST00000695689.1:c.518-59_518-57del	ENSP00000512101.1:n.518-59_518-57del
ENST00000695690.1:n.1612-59_1612-57del
ENST00000695691.1:n.1408-59_1408-57del
ENST00000245907.11:c.4547-59_4547-57del MANE Select	ENSP00000245907.4:n.4547-59_4547-57del
ENST00000245907.10:c.4547-59_4547-57del	ENSP00000245907.4:n.4547-59_4547-57del
ENST00000599668.1:n.167-59_167-57del
ENST00000599899.5:n.1506-59_1506-57del
ENST00000601008.1:c.242-1309_242-1307del	ENSP00000471384.1:n.242-1309_242-1307del
NM_000064.3:c.4547-59_4547-57del	NP_000055.2:n.4547-59_4547-57del
NM_000064.4:c.4547-59_4547-57del MANE Select	NP_000055.2:n.4547-59_4547-57del