Canonical Allele Identifier: CA403612856

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679496T>A (hg19) ; chr19:g.6679485T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679485T>A , CM000681.2:g.6679485T>A	GRCh38
NC_000019.9:g.6679496T>A , CM000681.1:g.6679496T>A	GRCh37
NC_000019.8:g.6630496T>A	NCBI36
NG_009557.1:g.46167A>T , LRG_27:g.46167A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2816A>T
ENST00000695653.1:c.2377A>T	ENSP00000512084.1:p.Thr793Ser
ENST00000695654.1:c.3493A>T	ENSP00000512085.1:p.Thr1165Ser
ENST00000695689.1:c.439A>T	ENSP00000512101.1:n.439A>T
ENST00000695690.1:n.1533A>T
ENST00000695691.1:n.1329A>T
ENST00000245907.11:c.4468A>T MANE Select	ENSP00000245907.4:p.Thr1490Ser
ENST00000245907.10:c.4468A>T	ENSP00000245907.4:p.Thr1490Ser
ENST00000599668.1:n.63A>T
ENST00000599899.5:n.1427A>T
ENST00000601008.1:c.242-1527A>T	ENSP00000471384.1:n.242-1527A>T
NM_000064.3:c.4468A>T	NP_000055.2:p.Thr1490Ser
NM_000064.4:c.4468A>T MANE Select	NP_000055.2:p.Thr1490Ser