Canonical Allele Identifier: CA993073365

Gene: C3

Linked Data

• gnomAD v3: 19-6709988-A-AGG
• gnomAD v4: 19-6709988-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709989_6709990insGG , CM000681.2:g.6709989_6709990insGG	GRCh38
NC_000019.9:g.6710000_6710001insGG , CM000681.1:g.6710000_6710001insGG	GRCh37
NC_000019.8:g.6661000_6661001insGG	NCBI36
NG_009557.1:g.15663_15664insCC , LRG_27:g.15663_15664insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-147_1564-146insCC	ENSP00000512083.1:n.1564-147_1564-146insCC
ENST00000695654.1:c.811-147_811-146insCC	ENSP00000512085.1:n.811-147_811-146insCC
ENST00000695655.1:c.592-111_592-110insCC	ENSP00000512086.1:n.592-111_592-110insCC
ENST00000695692.1:n.1051-147_1051-146insCC
ENST00000245907.11:c.1687-147_1687-146insCC MANE Select	ENSP00000245907.4:n.1687-147_1687-146insCC
ENST00000245907.10:c.1687-147_1687-146insCC	ENSP00000245907.4:n.1687-147_1687-146insCC
ENST00000600763.1:n.320-147_320-146insCC
NM_000064.3:c.1687-147_1687-146insCC	NP_000055.2:n.1687-147_1687-146insCC
NM_000064.4:c.1687-147_1687-146insCC MANE Select	NP_000055.2:n.1687-147_1687-146insCC