Canonical Allele Identifier: CA403612582

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679426C>T (hg19) ; chr19:g.6679415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679415C>T , CM000681.2:g.6679415C>T	GRCh38
NC_000019.9:g.6679426C>T , CM000681.1:g.6679426C>T	GRCh37
NC_000019.8:g.6630426C>T	NCBI36
NG_009557.1:g.46237G>A , LRG_27:g.46237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2886G>A
ENST00000695653.1:c.2447G>A	ENSP00000512084.1:p.Cys816Tyr
ENST00000695654.1:c.3563G>A	ENSP00000512085.1:p.Cys1188Tyr
ENST00000695689.1:c.509G>A	ENSP00000512101.1:n.509G>A
ENST00000695690.1:n.1603G>A
ENST00000695691.1:n.1399G>A
ENST00000245907.11:c.4538G>A MANE Select	ENSP00000245907.4:p.Cys1513Tyr
ENST00000245907.10:c.4538G>A	ENSP00000245907.4:p.Cys1513Tyr
ENST00000599668.1:n.133G>A
ENST00000599899.5:n.1497G>A
ENST00000601008.1:c.242-1457G>A	ENSP00000471384.1:n.242-1457G>A
NM_000064.3:c.4538G>A	NP_000055.2:p.Cys1513Tyr
NM_000064.4:c.4538G>A MANE Select	NP_000055.2:p.Cys1513Tyr