Canonical Allele Identifier: CA403615362

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682184C>G (hg19) ; chr19:g.6682173C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682173C>G , CM000681.2:g.6682173C>G	GRCh38
NC_000019.9:g.6682184C>G , CM000681.1:g.6682184C>G	GRCh37
NC_000019.8:g.6633184C>G	NCBI36
NG_009557.1:g.43479G>C , LRG_27:g.43479G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2577G>C
ENST00000695653.1:c.2138G>C	ENSP00000512084.1:p.Gly713Ala
ENST00000695654.1:c.3254G>C	ENSP00000512085.1:p.Gly1085Ala
ENST00000695689.1:c.200G>C	ENSP00000512101.1:n.200G>C
ENST00000695690.1:n.420G>C
ENST00000695691.1:n.420G>C
ENST00000245907.11:c.4229G>C MANE Select	ENSP00000245907.4:p.Gly1410Ala
ENST00000245907.10:c.4229G>C	ENSP00000245907.4:p.Gly1410Ala
ENST00000596548.1:c.350G>C	ENSP00000469744.1:p.Gly117Ala
ENST00000599899.5:n.1188G>C
ENST00000601008.1:c.242-4215G>C	ENSP00000471384.1:n.242-4215G>C
NM_000064.3:c.4229G>C	NP_000055.2:p.Gly1410Ala
NM_000064.4:c.4229G>C MANE Select	NP_000055.2:p.Gly1410Ala