Canonical Allele Identifier: CA403634172

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697794C>G (hg19) ; chr19:g.6697783C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697783C>G , CM000681.2:g.6697783C>G	GRCh38
NC_000019.9:g.6697794C>G , CM000681.1:g.6697794C>G	GRCh37
NC_000019.8:g.6648794C>G	NCBI36
NG_009557.1:g.27869G>C , LRG_27:g.27869G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.800G>C
ENST00000695652.1:c.2329G>C	ENSP00000512083.1:p.Ala777Pro
ENST00000695653.1:c.361G>C	ENSP00000512084.1:p.Ala121Pro
ENST00000695654.1:c.1576G>C	ENSP00000512085.1:p.Ala526Pro
ENST00000695655.1:c.1393G>C	ENSP00000512086.1:n.1393G>C
ENST00000695692.1:n.1816G>C
ENST00000245907.11:c.2452G>C MANE Select	ENSP00000245907.4:p.Ala818Pro
ENST00000245907.10:c.2452G>C	ENSP00000245907.4:p.Ala818Pro
ENST00000602053.1:n.500G>C
NM_000064.3:c.2452G>C	NP_000055.2:p.Ala818Pro
NM_000064.4:c.2452G>C MANE Select	NP_000055.2:p.Ala818Pro