Canonical Allele Identifier: CA505192508

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697726A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697715A>G , CM000681.2:g.6697715A>G	GRCh38
NC_000019.9:g.6697726A>G , CM000681.1:g.6697726A>G	GRCh37
NC_000019.8:g.6648726A>G	NCBI36
NG_009557.1:g.27937T>C , LRG_27:g.27937T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.868T>C
ENST00000695652.1:c.2397T>C	ENSP00000512083.1:p.Val799=
ENST00000695653.1:c.429T>C	ENSP00000512084.1:p.Val143=
ENST00000695654.1:c.1644T>C	ENSP00000512085.1:p.Val548=
ENST00000695655.1:c.1461T>C	ENSP00000512086.1:n.1461T>C
ENST00000695692.1:n.1884T>C
ENST00000245907.11:c.2520T>C MANE Select	ENSP00000245907.4:p.Val840=
ENST00000245907.10:c.2520T>C	ENSP00000245907.4:p.Val840=
ENST00000594005.1:n.1T>C
ENST00000602053.1:n.568T>C
NM_000064.3:c.2520T>C	NP_000055.2:p.Val840=
NM_000064.4:c.2520T>C MANE Select	NP_000055.2:p.Val840=