Canonical Allele Identifier: CA631722449

Gene: C3

Linked Data

• dbSNP Id: rs1244573146
• gnomAD v2: 19-6709977-GGGGAGAGAGA-G
• gnomAD v3: 19-6709966-GGGGAGAGAGA-G
• gnomAD v4: 19-6709966-GGGGAGAGAGA-G
• MyVariant Identifiers: chr19:g.6709978_6709987del (hg19) ; chr19:g.6709967_6709976del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709978_6709987del , CM000681.2:g.6709978_6709987del	GRCh38
NC_000019.9:g.6709989_6709998del , CM000681.1:g.6709989_6709998del	GRCh37
NC_000019.8:g.6660989_6660998del	NCBI36
NG_009557.1:g.15676_15685del , LRG_27:g.15676_15685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-134_1564-125del	ENSP00000512083.1:n.1564-134_1564-125del
ENST00000695654.1:c.811-134_811-125del	ENSP00000512085.1:n.811-134_811-125del
ENST00000695655.1:c.592-98_592-89del	ENSP00000512086.1:n.592-98_592-89del
ENST00000695692.1:n.1051-134_1051-125del
ENST00000245907.11:c.1687-134_1687-125del MANE Select	ENSP00000245907.4:n.1687-134_1687-125del
ENST00000245907.10:c.1687-134_1687-125del	ENSP00000245907.4:n.1687-134_1687-125del
ENST00000600763.1:n.320-134_320-125del
NM_000064.3:c.1687-134_1687-125del	NP_000055.2:n.1687-134_1687-125del
NM_000064.4:c.1687-134_1687-125del MANE Select	NP_000055.2:n.1687-134_1687-125del