Canonical Allele Identifier: CA403633977

Gene: C3

Linked Data

• ClinVar Variation Id: 1381215
• ClinVar RCV Id: RCV001886581
• dbSNP Id: rs2145412016
• MyVariant Identifiers: chr19:g.6697734A>T (hg19) ; chr19:g.6697723A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697723A>T , CM000681.2:g.6697723A>T	GRCh38
NC_000019.9:g.6697734A>T , CM000681.1:g.6697734A>T	GRCh37
NC_000019.8:g.6648734A>T	NCBI36
NG_009557.1:g.27929T>A , LRG_27:g.27929T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.860T>A
ENST00000695652.1:c.2389T>A	ENSP00000512083.1:p.Ser797Thr
ENST00000695653.1:c.421T>A	ENSP00000512084.1:p.Ser141Thr
ENST00000695654.1:c.1636T>A	ENSP00000512085.1:p.Ser546Thr
ENST00000695655.1:c.1453T>A	ENSP00000512086.1:n.1453T>A
ENST00000695692.1:n.1876T>A
ENST00000245907.11:c.2512T>A MANE Select	ENSP00000245907.4:p.Ser838Thr
ENST00000245907.10:c.2512T>A	ENSP00000245907.4:p.Ser838Thr
ENST00000602053.1:n.560T>A
NM_000064.3:c.2512T>A	NP_000055.2:p.Ser838Thr
NM_000064.4:c.2512T>A MANE Select	NP_000055.2:p.Ser838Thr