Canonical Allele Identifier: CA631722462

Gene: C3

Linked Data

• dbSNP Id: rs1164286633
• gnomAD v2: 19-6710036-GCGGGAGAGAGAGAGAA-G
• gnomAD v3: 19-6710025-GCGGGAGAGAGAGAGAA-G
• gnomAD v4: 19-6710025-GCGGGAGAGAGAGAGAA-G
• MyVariant Identifiers: chr19:g.6710037_6710052del (hg19) ; chr19:g.6710026_6710041del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710026_6710041del , CM000681.2:g.6710026_6710041del	GRCh38
NC_000019.9:g.6710037_6710052del , CM000681.1:g.6710037_6710052del	GRCh37
NC_000019.8:g.6661037_6661052del	NCBI36
NG_009557.1:g.15611_15626del , LRG_27:g.15611_15626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-199_1564-184del	ENSP00000512083.1:n.1564-199_1564-184del
ENST00000695654.1:c.811-199_811-184del	ENSP00000512085.1:n.811-199_811-184del
ENST00000695655.1:c.592-163_592-148del	ENSP00000512086.1:n.592-163_592-148del
ENST00000695692.1:n.1051-199_1051-184del
ENST00000245907.11:c.1687-199_1687-184del MANE Select	ENSP00000245907.4:n.1687-199_1687-184del
ENST00000245907.10:c.1687-199_1687-184del	ENSP00000245907.4:n.1687-199_1687-184del
ENST00000600763.1:n.320-199_320-184del
NM_000064.3:c.1687-199_1687-184del	NP_000055.2:n.1687-199_1687-184del
NM_000064.4:c.1687-199_1687-184del MANE Select	NP_000055.2:n.1687-199_1687-184del