Canonical Allele Identifier: CA2587877222

Gene: C3

Linked Data

• gnomAD v4: 19-6709614-C-CCCCCCCCCCCCCCCCCCCCCCCCCCCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709614_6709615insCCCCCCCCCCCCCCCCCCCCCCCCCCCG , CM000681.2:g.6709614_6709615insCCCCCCCCCCCCCCCCCCCCCCCCCCCG	GRCh38
NC_000019.9:g.6709625_6709626insCCCCCCCCCCCCCCCCCCCCCCCCCCCG , CM000681.1:g.6709625_6709626insCCCCCCCCCCCCCCCCCCCCCCCCCCCG	GRCh37
NC_000019.8:g.6660625_6660626insCCCCCCCCCCCCCCCCCCCCCCCCCCCG	NCBI36
NG_009557.1:g.16037_16038insCGGGGGGGGGGGGGGGGGGGGGGGGGGG , LRG_27:g.16037_16038insCGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+69_1722+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000512083.1:n.1722+69_1722+70insCGGGGGGGGGGGGGGGGGGGGGG...
ENST00000695654.1:c.969+69_969+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000512085.1:n.969+69_969+70insCGGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000695655.1:c.786+69_786+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000512086.1:n.786+69_786+70insCGGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000695692.1:n.1209+69_1209+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000245907.11:c.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000245907.4:n.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGG...
ENST00000245907.10:c.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000245907.4:n.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGG...
NM_000064.3:c.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG	NP_000055.2:n.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_000064.4:c.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_000055.2:n.1845+69_1845+70insCGGGGGGGGGGGGGGGGGGGGGGGGGGG