Canonical Allele Identifier: CA403612555

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679421C>T (hg19) ; chr19:g.6679410C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679410C>T , CM000681.2:g.6679410C>T	GRCh38
NC_000019.9:g.6679421C>T , CM000681.1:g.6679421C>T	GRCh37
NC_000019.8:g.6630421C>T	NCBI36
NG_009557.1:g.46242G>A , LRG_27:g.46242G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2891G>A
ENST00000695653.1:c.2452G>A	ENSP00000512084.1:p.Glu818Lys
ENST00000695654.1:c.3568G>A	ENSP00000512085.1:p.Glu1190Lys
ENST00000695689.1:c.514G>A	ENSP00000512101.1:n.514G>A
ENST00000695690.1:n.1608G>A
ENST00000695691.1:n.1404G>A
ENST00000245907.11:c.4543G>A MANE Select	ENSP00000245907.4:p.Glu1515Lys
ENST00000245907.10:c.4543G>A	ENSP00000245907.4:p.Glu1515Lys
ENST00000599668.1:n.138G>A
ENST00000599899.5:n.1502G>A
ENST00000601008.1:c.242-1452G>A	ENSP00000471384.1:n.242-1452G>A
NM_000064.3:c.4543G>A	NP_000055.2:p.Glu1515Lys
NM_000064.4:c.4543G>A MANE Select	NP_000055.2:p.Glu1515Lys