Canonical Allele Identifier: CA505192449

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697678C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697667C>T , CM000681.2:g.6697667C>T	GRCh38
NC_000019.9:g.6697678C>T , CM000681.1:g.6697678C>T	GRCh37
NC_000019.8:g.6648678C>T	NCBI36
NG_009557.1:g.27985G>A , LRG_27:g.27985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.916G>A
ENST00000695652.1:c.2445G>A	ENSP00000512083.1:p.Gln815=
ENST00000695653.1:c.477G>A	ENSP00000512084.1:p.Gln159=
ENST00000695654.1:c.1692G>A	ENSP00000512085.1:p.Gln564=
ENST00000695655.1:c.1509G>A	ENSP00000512086.1:n.1509G>A
ENST00000695692.1:n.1932G>A
ENST00000245907.11:c.2568G>A MANE Select	ENSP00000245907.4:p.Gln856=
ENST00000245907.10:c.2568G>A	ENSP00000245907.4:p.Gln856=
ENST00000594005.1:n.49G>A
ENST00000602053.1:n.616G>A
NM_000064.3:c.2568G>A	NP_000055.2:p.Gln856=
NM_000064.4:c.2568G>A MANE Select	NP_000055.2:p.Gln856=