Canonical Allele Identifier: CA505124513

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697798A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697787A>G , CM000681.2:g.6697787A>G	GRCh38
NC_000019.9:g.6697798A>G , CM000681.1:g.6697798A>G	GRCh37
NC_000019.8:g.6648798A>G	NCBI36
NG_009557.1:g.27865T>C , LRG_27:g.27865T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.796T>C
ENST00000695652.1:c.2325T>C	ENSP00000512083.1:p.Cys775=
ENST00000695653.1:c.357T>C	ENSP00000512084.1:p.Cys119=
ENST00000695654.1:c.1572T>C	ENSP00000512085.1:p.Cys524=
ENST00000695655.1:c.1389T>C	ENSP00000512086.1:n.1389T>C
ENST00000695692.1:n.1812T>C
ENST00000245907.11:c.2448T>C MANE Select	ENSP00000245907.4:p.Cys816=
ENST00000245907.10:c.2448T>C	ENSP00000245907.4:p.Cys816=
ENST00000602053.1:n.496T>C
NM_000064.3:c.2448T>C	NP_000055.2:p.Cys816=
NM_000064.4:c.2448T>C MANE Select	NP_000055.2:p.Cys816=