Canonical Allele Identifier: CA631722459

Gene: C3

Linked Data

• dbSNP Id: rs1444144218
• gnomAD v2: 19-6710015-AGGGAGAGAGAGGGAGAGAGGGC-A
• gnomAD v3: 19-6710004-AGGGAGAGAGAGGGAGAGAGGGC-A
• gnomAD v4: 19-6710004-AGGGAGAGAGAGGGAGAGAGGGC-A
• MyVariant Identifiers: chr19:g.6710016_6710037del (hg19) ; chr19:g.6710005_6710026del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710016_6710037del , CM000681.2:g.6710016_6710037del	GRCh38
NC_000019.9:g.6710027_6710048del , CM000681.1:g.6710027_6710048del	GRCh37
NC_000019.8:g.6661027_6661048del	NCBI36
NG_009557.1:g.15626_15647del , LRG_27:g.15626_15647del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-184_1564-163del	ENSP00000512083.1:n.1564-184_1564-163del
ENST00000695654.1:c.811-184_811-163del	ENSP00000512085.1:n.811-184_811-163del
ENST00000695655.1:c.592-148_592-127del	ENSP00000512086.1:n.592-148_592-127del
ENST00000695692.1:n.1051-184_1051-163del
ENST00000245907.11:c.1687-184_1687-163del MANE Select	ENSP00000245907.4:n.1687-184_1687-163del
ENST00000245907.10:c.1687-184_1687-163del	ENSP00000245907.4:n.1687-184_1687-163del
ENST00000600763.1:n.320-184_320-163del
NM_000064.3:c.1687-184_1687-163del	NP_000055.2:n.1687-184_1687-163del
NM_000064.4:c.1687-184_1687-163del MANE Select	NP_000055.2:n.1687-184_1687-163del