Canonical Allele Identifier: CA403619902

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686245A>T (hg19) ; chr19:g.6686234A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686234A>T , CM000681.2:g.6686234A>T	GRCh38
NC_000019.9:g.6686245A>T , CM000681.1:g.6686245A>T	GRCh37
NC_000019.8:g.6637245A>T	NCBI36
NG_009557.1:g.39418T>A , LRG_27:g.39418T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2048T>A
ENST00000695652.1:c.3577T>A	ENSP00000512083.1:p.Ser1193Thr
ENST00000695653.1:c.1609T>A	ENSP00000512084.1:p.Ser537Thr
ENST00000695654.1:c.2725T>A	ENSP00000512085.1:p.Ser909Thr
ENST00000695655.1:c.2641T>A	ENSP00000512086.1:n.2641T>A
ENST00000695692.1:n.3064T>A
ENST00000245907.11:c.3700T>A MANE Select	ENSP00000245907.4:p.Ser1234Thr
ENST00000245907.10:c.3700T>A	ENSP00000245907.4:p.Ser1234Thr
ENST00000596238.1:n.143T>A
ENST00000601008.1:c.241+512T>A	ENSP00000471384.1:n.241+512T>A
NM_000064.3:c.3700T>A	NP_000055.2:p.Ser1234Thr
NM_000064.4:c.3700T>A MANE Select	NP_000055.2:p.Ser1234Thr