Canonical Allele Identifier: CA403633021

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697476G>T (hg19) ; chr19:g.6697465G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697465G>T , CM000681.2:g.6697465G>T	GRCh38
NC_000019.9:g.6697476G>T , CM000681.1:g.6697476G>T	GRCh37
NC_000019.8:g.6648476G>T	NCBI36
NG_009557.1:g.28187C>A , LRG_27:g.28187C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1023C>A
ENST00000695652.1:c.2552C>A	ENSP00000512083.1:p.Ser851Tyr
ENST00000695653.1:c.584C>A	ENSP00000512084.1:p.Ser195Tyr
ENST00000695654.1:c.1799C>A	ENSP00000512085.1:p.Ser600Tyr
ENST00000695655.1:c.1616C>A	ENSP00000512086.1:n.1616C>A
ENST00000695692.1:n.2039C>A
ENST00000245907.11:c.2675C>A MANE Select	ENSP00000245907.4:p.Ser892Tyr
ENST00000245907.10:c.2675C>A	ENSP00000245907.4:p.Ser892Tyr
ENST00000594005.1:n.251C>A
NM_000064.3:c.2675C>A	NP_000055.2:p.Ser892Tyr
NM_000064.4:c.2675C>A MANE Select	NP_000055.2:p.Ser892Tyr