Canonical Allele Identifier: CA403612884

Gene: C3

Linked Data

• gnomAD v4: 19-6679496-T-C
• MyVariant Identifiers: chr19:g.6679507T>C (hg19) ; chr19:g.6679496T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679496T>C , CM000681.2:g.6679496T>C	GRCh38
NC_000019.9:g.6679507T>C , CM000681.1:g.6679507T>C	GRCh37
NC_000019.8:g.6630507T>C	NCBI36
NG_009557.1:g.46156A>G , LRG_27:g.46156A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805A>G
ENST00000695653.1:c.2366A>G	ENSP00000512084.1:p.Glu789Gly
ENST00000695654.1:c.3482A>G	ENSP00000512085.1:p.Glu1161Gly
ENST00000695689.1:c.428A>G	ENSP00000512101.1:n.428A>G
ENST00000695690.1:n.1522A>G
ENST00000695691.1:n.1318A>G
ENST00000245907.11:c.4457A>G MANE Select	ENSP00000245907.4:p.Glu1486Gly
ENST00000245907.10:c.4457A>G	ENSP00000245907.4:p.Glu1486Gly
ENST00000599668.1:n.52A>G
ENST00000599899.5:n.1416A>G
ENST00000601008.1:c.242-1538A>G	ENSP00000471384.1:n.242-1538A>G
NM_000064.3:c.4457A>G	NP_000055.2:p.Glu1486Gly
NM_000064.4:c.4457A>G MANE Select	NP_000055.2:p.Glu1486Gly