Canonical Allele Identifier: CA403639328

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709753A>T (hg19) ; chr19:g.6709742A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709742A>T , CM000681.2:g.6709742A>T	GRCh38
NC_000019.9:g.6709753A>T , CM000681.1:g.6709753A>T	GRCh37
NC_000019.8:g.6660753A>T	NCBI36
NG_009557.1:g.15910T>A , LRG_27:g.15910T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1664T>A	ENSP00000512083.1:p.Val555Glu
ENST00000695654.1:c.911T>A	ENSP00000512085.1:p.Val304Glu
ENST00000695655.1:c.728T>A	ENSP00000512086.1:n.728T>A
ENST00000695692.1:n.1151T>A
ENST00000245907.11:c.1787T>A MANE Select	ENSP00000245907.4:p.Val596Glu
ENST00000245907.10:c.1787T>A	ENSP00000245907.4:p.Val596Glu
NM_000064.3:c.1787T>A	NP_000055.2:p.Val596Glu
NM_000064.4:c.1787T>A MANE Select	NP_000055.2:p.Val596Glu