Canonical Allele Identifier: CA403610765

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6678028G>T (hg19) ; chr19:g.6678017G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6678017G>T , CM000681.2:g.6678017G>T	GRCh38
NC_000019.9:g.6678028G>T , CM000681.1:g.6678028G>T	GRCh37
NC_000019.8:g.6629028G>T	NCBI36
NG_009557.1:g.47635C>A , LRG_27:g.47635C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.3205C>A
ENST00000695653.1:c.2766C>A	ENSP00000512084.1:p.Ser922Arg
ENST00000695654.1:c.3882C>A	ENSP00000512085.1:p.Ser1294Arg
ENST00000695689.1:c.828C>A	ENSP00000512101.1:n.828C>A
ENST00000695690.1:n.1922C>A
ENST00000695691.1:n.1718C>A
ENST00000245907.11:c.4857C>A MANE Select	ENSP00000245907.4:p.Ser1619Arg
ENST00000245907.10:c.4857C>A	ENSP00000245907.4:p.Ser1619Arg
ENST00000599668.1:n.477C>A
ENST00000599899.5:n.1816C>A
ENST00000601008.1:c.242-59C>A	ENSP00000471384.1:n.242-59C>A
ENST00000601475.1:n.186C>A
ENST00000602229.1:c.432C>A
NM_000064.3:c.4857C>A	NP_000055.2:p.Ser1619Arg
NM_000064.4:c.4857C>A MANE Select	NP_000055.2:p.Ser1619Arg