Canonical Allele Identifier: CA884140900

Gene: C3

Linked Data

• dbSNP Id: rs1367807457
• MyVariant Identifiers: chr19:g.6698012A>T (hg19) ; chr19:g.6698001A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698001A>T , CM000681.2:g.6698001A>T	GRCh38
NC_000019.9:g.6698012A>T , CM000681.1:g.6698012A>T	GRCh37
NC_000019.8:g.6649012A>T	NCBI36
NG_009557.1:g.27651T>A , LRG_27:g.27651T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-207T>A
ENST00000695652.1:c.2318-207T>A	ENSP00000512083.1:n.2318-207T>A
ENST00000695653.1:c.350-207T>A	ENSP00000512084.1:n.350-207T>A
ENST00000695654.1:c.1565-207T>A	ENSP00000512085.1:n.1565-207T>A
ENST00000695655.1:c.1382-207T>A	ENSP00000512086.1:n.1382-207T>A
ENST00000695692.1:n.1805-207T>A
ENST00000245907.11:c.2441-207T>A MANE Select	ENSP00000245907.4:n.2441-207T>A
ENST00000245907.10:c.2441-207T>A	ENSP00000245907.4:n.2441-207T>A
ENST00000602053.1:n.489-207T>A
NM_000064.3:c.2441-207T>A	NP_000055.2:n.2441-207T>A
NM_000064.4:c.2441-207T>A MANE Select	NP_000055.2:n.2441-207T>A