Canonical Allele Identifier: CA403612248

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679198G>T (hg19) ; chr19:g.6679187G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679187G>T , CM000681.2:g.6679187G>T	GRCh38
NC_000019.9:g.6679198G>T , CM000681.1:g.6679198G>T	GRCh37
NC_000019.8:g.6630198G>T	NCBI36
NG_009557.1:g.46465C>A , LRG_27:g.46465C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2916C>A
ENST00000695653.1:c.2477C>A	ENSP00000512084.1:p.Ser826Ter
ENST00000695654.1:c.3593C>A	ENSP00000512085.1:p.Ser1198Ter
ENST00000695689.1:c.539C>A	ENSP00000512101.1:n.539C>A
ENST00000695690.1:n.1633C>A
ENST00000695691.1:n.1429C>A
ENST00000245907.11:c.4568C>A MANE Select	ENSP00000245907.4:p.Ser1523Ter
ENST00000245907.10:c.4568C>A	ENSP00000245907.4:p.Ser1523Ter
ENST00000599668.1:n.188C>A
ENST00000599899.5:n.1527C>A
ENST00000601008.1:c.242-1229C>A	ENSP00000471384.1:n.242-1229C>A
ENST00000602229.1:c.15C>A
NM_000064.3:c.4568C>A	NP_000055.2:p.Ser1523Ter
NM_000064.4:c.4568C>A MANE Select	NP_000055.2:p.Ser1523Ter