Canonical Allele Identifier: CA403614675

Gene: C3

Linked Data

• gnomAD v4: 19-6681971-A-T
• MyVariant Identifiers: chr19:g.6681982A>T (hg19) ; chr19:g.6681971A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681971A>T , CM000681.2:g.6681971A>T	GRCh38
NC_000019.9:g.6681982A>T , CM000681.1:g.6681982A>T	GRCh37
NC_000019.8:g.6632982A>T	NCBI36
NG_009557.1:g.43681T>A , LRG_27:g.43681T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2668T>A
ENST00000695653.1:c.2229T>A	ENSP00000512084.1:p.Asp743Glu
ENST00000695654.1:c.3345T>A	ENSP00000512085.1:p.Asp1115Glu
ENST00000695689.1:c.291T>A	ENSP00000512101.1:n.291T>A
ENST00000695690.1:n.511T>A
ENST00000695691.1:n.511T>A
ENST00000245907.11:c.4320T>A MANE Select	ENSP00000245907.4:p.Asp1440Glu
ENST00000245907.10:c.4320T>A	ENSP00000245907.4:p.Asp1440Glu
ENST00000596548.1:c.441T>A	ENSP00000469744.1:p.Asp147Glu
ENST00000599899.5:n.1279T>A
ENST00000601008.1:c.242-4013T>A	ENSP00000471384.1:n.242-4013T>A
NM_000064.3:c.4320T>A	NP_000055.2:p.Asp1440Glu
NM_000064.4:c.4320T>A MANE Select	NP_000055.2:p.Asp1440Glu