Canonical Allele Identifier: CA2320561794

Gene: C3

Linked Data

• dbSNP Id: rs1599514204

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6701451A>C , CM000681.2:g.6701451A>C	GRCh38
NC_000019.9:g.6701462A>C , CM000681.1:g.6701462A>C	GRCh37
NC_000019.8:g.6652462A>C	NCBI36
NG_009557.1:g.24201T>G , LRG_27:g.24201T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.788+676T>G
ENST00000695652.1:c.2317+676T>G	ENSP00000512083.1:n.2317+676T>G
ENST00000695653.1:c.349+676T>G	ENSP00000512084.1:n.349+676T>G
ENST00000695654.1:c.1564+676T>G	ENSP00000512085.1:n.1564+676T>G
ENST00000695655.1:c.1381+676T>G	ENSP00000512086.1:n.1381+676T>G
ENST00000695692.1:n.1804+676T>G
ENST00000245907.11:c.2440+676T>G MANE Select	ENSP00000245907.4:n.2440+676T>G
ENST00000245907.10:c.2440+676T>G	ENSP00000245907.4:n.2440+676T>G
ENST00000602053.1:n.488+676T>G
NM_000064.3:c.2440+676T>G	NP_000055.2:n.2440+676T>G
NM_000064.4:c.2440+676T>G MANE Select	NP_000055.2:n.2440+676T>G