Canonical Allele Identifier: CA403614507

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6681962T>G (hg19) ; chr19:g.6681951T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681951T>G , CM000681.2:g.6681951T>G	GRCh38
NC_000019.9:g.6681962T>G , CM000681.1:g.6681962T>G	GRCh37
NC_000019.8:g.6632962T>G	NCBI36
NG_009557.1:g.43701A>C , LRG_27:g.43701A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2688A>C
ENST00000695653.1:c.2249A>C	ENSP00000512084.1:p.Tyr750Ser
ENST00000695654.1:c.3365A>C	ENSP00000512085.1:p.Tyr1122Ser
ENST00000695689.1:c.311A>C	ENSP00000512101.1:n.311A>C
ENST00000695690.1:n.531A>C
ENST00000695691.1:n.531A>C
ENST00000245907.11:c.4340A>C MANE Select	ENSP00000245907.4:p.Tyr1447Ser
ENST00000245907.10:c.4340A>C	ENSP00000245907.4:p.Tyr1447Ser
ENST00000596548.1:c.461A>C	ENSP00000469744.1:p.Tyr154Ser
ENST00000599899.5:n.1299A>C
ENST00000601008.1:c.242-3993A>C	ENSP00000471384.1:n.242-3993A>C
NM_000064.3:c.4340A>C	NP_000055.2:p.Tyr1447Ser
NM_000064.4:c.4340A>C MANE Select	NP_000055.2:p.Tyr1447Ser