Canonical Allele Identifier: CA884148719

Gene: C3

Linked Data

• dbSNP Id: rs1254657157
• gnomAD v3: 19-6709994-GGAGAGAGGGAGGGA-G
• gnomAD v4: 19-6709994-GGAGAGAGGGAGGGA-G
• MyVariant Identifiers: chr19:g.6710006_6710019del (hg19) ; chr19:g.6709995_6710008del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710006_6710019del , CM000681.2:g.6710006_6710019del	GRCh38
NC_000019.9:g.6710017_6710030del , CM000681.1:g.6710017_6710030del	GRCh37
NC_000019.8:g.6661017_6661030del	NCBI36
NG_009557.1:g.15644_15657del , LRG_27:g.15644_15657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-166_1564-153del	ENSP00000512083.1:n.1564-166_1564-153del
ENST00000695654.1:c.811-166_811-153del	ENSP00000512085.1:n.811-166_811-153del
ENST00000695655.1:c.592-130_592-117del	ENSP00000512086.1:n.592-130_592-117del
ENST00000695692.1:n.1051-166_1051-153del
ENST00000245907.11:c.1687-166_1687-153del MANE Select	ENSP00000245907.4:n.1687-166_1687-153del
ENST00000245907.10:c.1687-166_1687-153del	ENSP00000245907.4:n.1687-166_1687-153del
ENST00000600763.1:n.320-166_320-153del
NM_000064.3:c.1687-166_1687-153del	NP_000055.2:n.1687-166_1687-153del
NM_000064.4:c.1687-166_1687-153del MANE Select	NP_000055.2:n.1687-166_1687-153del