Canonical Allele Identifier: CA505119974

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679170C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679159C>G , CM000681.2:g.6679159C>G	GRCh38
NC_000019.9:g.6679170C>G , CM000681.1:g.6679170C>G	GRCh37
NC_000019.8:g.6630170C>G	NCBI36
NG_009557.1:g.46493G>C , LRG_27:g.46493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2944G>C
ENST00000695653.1:c.2505G>C	ENSP00000512084.1:p.Arg835=
ENST00000695654.1:c.3621G>C	ENSP00000512085.1:p.Arg1207=
ENST00000695689.1:c.567G>C	ENSP00000512101.1:n.567G>C
ENST00000695690.1:n.1661G>C
ENST00000695691.1:n.1457G>C
ENST00000245907.11:c.4596G>C MANE Select	ENSP00000245907.4:p.Arg1532=
ENST00000245907.10:c.4596G>C	ENSP00000245907.4:p.Arg1532=
ENST00000599668.1:n.216G>C
ENST00000599899.5:n.1555G>C
ENST00000601008.1:c.242-1201G>C	ENSP00000471384.1:n.242-1201G>C
ENST00000602229.1:c.43G>C
NM_000064.3:c.4596G>C	NP_000055.2:p.Arg1532=
NM_000064.4:c.4596G>C MANE Select	NP_000055.2:p.Arg1532=