Canonical Allele Identifier: CA403612037

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679157A>T (hg19) ; chr19:g.6679146A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679146A>T , CM000681.2:g.6679146A>T	GRCh38
NC_000019.9:g.6679157A>T , CM000681.1:g.6679157A>T	GRCh37
NC_000019.8:g.6630157A>T	NCBI36
NG_009557.1:g.46506T>A , LRG_27:g.46506T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2957T>A
ENST00000695653.1:c.2518T>A	ENSP00000512084.1:p.Cys840Ser
ENST00000695654.1:c.3634T>A	ENSP00000512085.1:p.Cys1212Ser
ENST00000695689.1:c.580T>A	ENSP00000512101.1:n.580T>A
ENST00000695690.1:n.1674T>A
ENST00000695691.1:n.1470T>A
ENST00000245907.11:c.4609T>A MANE Select	ENSP00000245907.4:p.Cys1537Ser
ENST00000245907.10:c.4609T>A	ENSP00000245907.4:p.Cys1537Ser
ENST00000599668.1:n.229T>A
ENST00000599899.5:n.1568T>A
ENST00000601008.1:c.242-1188T>A	ENSP00000471384.1:n.242-1188T>A
ENST00000602229.1:c.56T>A
NM_000064.3:c.4609T>A	NP_000055.2:p.Cys1537Ser
NM_000064.4:c.4609T>A MANE Select	NP_000055.2:p.Cys1537Ser