Canonical Allele Identifier: CA403633853

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697697A>C (hg19) ; chr19:g.6697686A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697686A>C , CM000681.2:g.6697686A>C	GRCh38
NC_000019.9:g.6697697A>C , CM000681.1:g.6697697A>C	GRCh37
NC_000019.8:g.6648697A>C	NCBI36
NG_009557.1:g.27966T>G , LRG_27:g.27966T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.897T>G
ENST00000695652.1:c.2426T>G	ENSP00000512083.1:p.Val809Gly
ENST00000695653.1:c.458T>G	ENSP00000512084.1:p.Val153Gly
ENST00000695654.1:c.1673T>G	ENSP00000512085.1:p.Val558Gly
ENST00000695655.1:c.1490T>G	ENSP00000512086.1:n.1490T>G
ENST00000695692.1:n.1913T>G
ENST00000245907.11:c.2549T>G MANE Select	ENSP00000245907.4:p.Val850Gly
ENST00000245907.10:c.2549T>G	ENSP00000245907.4:p.Val850Gly
ENST00000594005.1:n.30T>G
ENST00000602053.1:n.597T>G
NM_000064.3:c.2549T>G	NP_000055.2:p.Val850Gly
NM_000064.4:c.2549T>G MANE Select	NP_000055.2:p.Val850Gly