Canonical Allele Identifier: CA403633981

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697736T>C (hg19) ; chr19:g.6697725T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697725T>C , CM000681.2:g.6697725T>C	GRCh38
NC_000019.9:g.6697736T>C , CM000681.1:g.6697736T>C	GRCh37
NC_000019.8:g.6648736T>C	NCBI36
NG_009557.1:g.27927A>G , LRG_27:g.27927A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.858A>G
ENST00000695652.1:c.2387A>G	ENSP00000512083.1:p.Tyr796Cys
ENST00000695653.1:c.419A>G	ENSP00000512084.1:p.Tyr140Cys
ENST00000695654.1:c.1634A>G	ENSP00000512085.1:p.Tyr545Cys
ENST00000695655.1:c.1451A>G	ENSP00000512086.1:n.1451A>G
ENST00000695692.1:n.1874A>G
ENST00000245907.11:c.2510A>G MANE Select	ENSP00000245907.4:p.Tyr837Cys
ENST00000245907.10:c.2510A>G	ENSP00000245907.4:p.Tyr837Cys
ENST00000602053.1:n.558A>G
NM_000064.3:c.2510A>G	NP_000055.2:p.Tyr837Cys
NM_000064.4:c.2510A>G MANE Select	NP_000055.2:p.Tyr837Cys