Canonical Allele Identifier: CA505192433

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697666G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697655G>T , CM000681.2:g.6697655G>T	GRCh38
NC_000019.9:g.6697666G>T , CM000681.1:g.6697666G>T	GRCh37
NC_000019.8:g.6648666G>T	NCBI36
NG_009557.1:g.27997C>A , LRG_27:g.27997C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.928C>A
ENST00000695652.1:c.2457C>A	ENSP00000512083.1:p.Leu819=
ENST00000695653.1:c.489C>A	ENSP00000512084.1:p.Leu163=
ENST00000695654.1:c.1704C>A	ENSP00000512085.1:p.Leu568=
ENST00000695655.1:c.1521C>A	ENSP00000512086.1:n.1521C>A
ENST00000695692.1:n.1944C>A
ENST00000245907.11:c.2580C>A MANE Select	ENSP00000245907.4:p.Leu860=
ENST00000245907.10:c.2580C>A	ENSP00000245907.4:p.Leu860=
ENST00000594005.1:n.61C>A
NM_000064.3:c.2580C>A	NP_000055.2:p.Leu860=
NM_000064.4:c.2580C>A MANE Select	NP_000055.2:p.Leu860=