Canonical Allele Identifier: CA2735579332

Gene: C3

Linked Data

• dbSNP Id: rs2145390510

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679383_6679387del , CM000681.2:g.6679383_6679387del	GRCh38
NC_000019.9:g.6679394_6679398del , CM000681.1:g.6679394_6679398del	GRCh37
NC_000019.8:g.6630394_6630398del	NCBI36
NG_009557.1:g.46266_46270del , LRG_27:g.46266_46270del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2894+21_2894+25del
ENST00000695653.1:c.2455+21_2455+25del	ENSP00000512084.1:n.2455+21_2455+25del
ENST00000695654.1:c.3571+21_3571+25del	ENSP00000512085.1:n.3571+21_3571+25del
ENST00000695689.1:c.517+21_517+25del	ENSP00000512101.1:n.517+21_517+25del
ENST00000695690.1:n.1611+21_1611+25del
ENST00000695691.1:n.1407+21_1407+25del
ENST00000245907.11:c.4546+21_4546+25del MANE Select	ENSP00000245907.4:n.4546+21_4546+25del
ENST00000245907.10:c.4546+21_4546+25del	ENSP00000245907.4:n.4546+21_4546+25del
ENST00000599668.1:n.162_166del
ENST00000599899.5:n.1505+21_1505+25del
ENST00000601008.1:c.242-1428_242-1424del	ENSP00000471384.1:n.242-1428_242-1424del
NM_000064.3:c.4546+21_4546+25del	NP_000055.2:n.4546+21_4546+25del
NM_000064.4:c.4546+21_4546+25del MANE Select	NP_000055.2:n.4546+21_4546+25del