Canonical Allele Identifier: CA505192464

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697696A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697685A>T , CM000681.2:g.6697685A>T	GRCh38
NC_000019.9:g.6697696A>T , CM000681.1:g.6697696A>T	GRCh37
NC_000019.8:g.6648696A>T	NCBI36
NG_009557.1:g.27967T>A , LRG_27:g.27967T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.898T>A
ENST00000695652.1:c.2427T>A	ENSP00000512083.1:p.Val809=
ENST00000695653.1:c.459T>A	ENSP00000512084.1:p.Val153=
ENST00000695654.1:c.1674T>A	ENSP00000512085.1:p.Val558=
ENST00000695655.1:c.1491T>A	ENSP00000512086.1:n.1491T>A
ENST00000695692.1:n.1914T>A
ENST00000245907.11:c.2550T>A MANE Select	ENSP00000245907.4:p.Val850=
ENST00000245907.10:c.2550T>A	ENSP00000245907.4:p.Val850=
ENST00000594005.1:n.31T>A
ENST00000602053.1:n.598T>A
NM_000064.3:c.2550T>A	NP_000055.2:p.Val850=
NM_000064.4:c.2550T>A MANE Select	NP_000055.2:p.Val850=