Canonical Allele Identifier: CA884148712

Gene: C3

Linked Data

• dbSNP Id: rs1366770206
• MyVariant Identifiers: chr19:g.6710003_6710014del (hg19) ; chr19:g.6709992_6710003del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710002_6710013del , CM000681.2:g.6710002_6710013del	GRCh38
NC_000019.9:g.6710013_6710024del , CM000681.1:g.6710013_6710024del	GRCh37
NC_000019.8:g.6661013_6661024del	NCBI36
NG_009557.1:g.15649_15660del , LRG_27:g.15649_15660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-161_1564-150del	ENSP00000512083.1:n.1564-161_1564-150del
ENST00000695654.1:c.811-161_811-150del	ENSP00000512085.1:n.811-161_811-150del
ENST00000695655.1:c.592-125_592-114del	ENSP00000512086.1:n.592-125_592-114del
ENST00000695692.1:n.1051-161_1051-150del
ENST00000245907.11:c.1687-161_1687-150del MANE Select	ENSP00000245907.4:n.1687-161_1687-150del
ENST00000245907.10:c.1687-161_1687-150del	ENSP00000245907.4:n.1687-161_1687-150del
ENST00000600763.1:n.320-161_320-150del
NM_000064.3:c.1687-161_1687-150del	NP_000055.2:n.1687-161_1687-150del
NM_000064.4:c.1687-161_1687-150del MANE Select	NP_000055.2:n.1687-161_1687-150del