Canonical Allele Identifier: CA2587877454

Gene: C3

Linked Data

• gnomAD v4: 19-6709634-A-ACCAACCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709634_6709635insCCAACCG , CM000681.2:g.6709634_6709635insCCAACCG	GRCh38
NC_000019.9:g.6709645_6709646insCCAACCG , CM000681.1:g.6709645_6709646insCCAACCG	GRCh37
NC_000019.8:g.6660645_6660646insCCAACCG	NCBI36
NG_009557.1:g.16017_16018insCGGTTGG , LRG_27:g.16017_16018insCGGTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+49_1722+50insCGGTTGG	ENSP00000512083.1:n.1722+49_1722+50insCGGTTGG
ENST00000695654.1:c.969+49_969+50insCGGTTGG	ENSP00000512085.1:n.969+49_969+50insCGGTTGG
ENST00000695655.1:c.786+49_786+50insCGGTTGG	ENSP00000512086.1:n.786+49_786+50insCGGTTGG
ENST00000695692.1:n.1209+49_1209+50insCGGTTGG
ENST00000245907.11:c.1845+49_1845+50insCGGTTGG MANE Select	ENSP00000245907.4:n.1845+49_1845+50insCGGTTGG
ENST00000245907.10:c.1845+49_1845+50insCGGTTGG	ENSP00000245907.4:n.1845+49_1845+50insCGGTTGG
NM_000064.3:c.1845+49_1845+50insCGGTTGG	NP_000055.2:n.1845+49_1845+50insCGGTTGG
NM_000064.4:c.1845+49_1845+50insCGGTTGG MANE Select	NP_000055.2:n.1845+49_1845+50insCGGTTGG