Canonical Allele Identifier: CA403614802

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6681997G>T (hg19) ; chr19:g.6681986G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681986G>T , CM000681.2:g.6681986G>T	GRCh38
NC_000019.9:g.6681997G>T , CM000681.1:g.6681997G>T	GRCh37
NC_000019.8:g.6632997G>T	NCBI36
NG_009557.1:g.43666C>A , LRG_27:g.43666C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2653C>A
ENST00000695653.1:c.2214C>A	ENSP00000512084.1:p.Asp738Glu
ENST00000695654.1:c.3330C>A	ENSP00000512085.1:p.Asp1110Glu
ENST00000695689.1:c.276C>A	ENSP00000512101.1:n.276C>A
ENST00000695690.1:n.496C>A
ENST00000695691.1:n.496C>A
ENST00000245907.11:c.4305C>A MANE Select	ENSP00000245907.4:p.Asp1435Glu
ENST00000245907.10:c.4305C>A	ENSP00000245907.4:p.Asp1435Glu
ENST00000596548.1:c.426C>A	ENSP00000469744.1:p.Asp142Glu
ENST00000599899.5:n.1264C>A
ENST00000601008.1:c.242-4028C>A	ENSP00000471384.1:n.242-4028C>A
NM_000064.3:c.4305C>A	NP_000055.2:p.Asp1435Glu
NM_000064.4:c.4305C>A MANE Select	NP_000055.2:p.Asp1435Glu