Canonical Allele Identifier: CA403611979

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679141T>C (hg19) ; chr19:g.6679130T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679130T>C , CM000681.2:g.6679130T>C	GRCh38
NC_000019.9:g.6679141T>C , CM000681.1:g.6679141T>C	GRCh37
NC_000019.8:g.6630141T>C	NCBI36
NG_009557.1:g.46522A>G , LRG_27:g.46522A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2973A>G
ENST00000695653.1:c.2534A>G	ENSP00000512084.1:p.Asp845Gly
ENST00000695654.1:c.3650A>G	ENSP00000512085.1:p.Asp1217Gly
ENST00000695689.1:c.596A>G	ENSP00000512101.1:n.596A>G
ENST00000695690.1:n.1690A>G
ENST00000695691.1:n.1486A>G
ENST00000245907.11:c.4625A>G MANE Select	ENSP00000245907.4:p.Asp1542Gly
ENST00000245907.10:c.4625A>G	ENSP00000245907.4:p.Asp1542Gly
ENST00000599668.1:n.245A>G
ENST00000599899.5:n.1584A>G
ENST00000601008.1:c.242-1172A>G	ENSP00000471384.1:n.242-1172A>G
ENST00000602229.1:c.72A>G
NM_000064.3:c.4625A>G	NP_000055.2:p.Asp1542Gly
NM_000064.4:c.4625A>G MANE Select	NP_000055.2:p.Asp1542Gly