Canonical Allele Identifier: CA403612715

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679448A>T (hg19) ; chr19:g.6679437A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679437A>T , CM000681.2:g.6679437A>T	GRCh38
NC_000019.9:g.6679448A>T , CM000681.1:g.6679448A>T	GRCh37
NC_000019.8:g.6630448A>T	NCBI36
NG_009557.1:g.46215T>A , LRG_27:g.46215T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2864T>A
ENST00000695653.1:c.2425T>A	ENSP00000512084.1:p.Cys809Ser
ENST00000695654.1:c.3541T>A	ENSP00000512085.1:p.Cys1181Ser
ENST00000695689.1:c.487T>A	ENSP00000512101.1:n.487T>A
ENST00000695690.1:n.1581T>A
ENST00000695691.1:n.1377T>A
ENST00000245907.11:c.4516T>A MANE Select	ENSP00000245907.4:p.Cys1506Ser
ENST00000245907.10:c.4516T>A	ENSP00000245907.4:p.Cys1506Ser
ENST00000599668.1:n.111T>A
ENST00000599899.5:n.1475T>A
ENST00000601008.1:c.242-1479T>A	ENSP00000471384.1:n.242-1479T>A
NM_000064.3:c.4516T>A	NP_000055.2:p.Cys1506Ser
NM_000064.4:c.4516T>A MANE Select	NP_000055.2:p.Cys1506Ser