Canonical Allele Identifier: CA505122446

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682236G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682225G>T , CM000681.2:g.6682225G>T	GRCh38
NC_000019.9:g.6682236G>T , CM000681.1:g.6682236G>T	GRCh37
NC_000019.8:g.6633236G>T	NCBI36
NG_009557.1:g.43427C>A , LRG_27:g.43427C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2525C>A
ENST00000695653.1:c.2086C>A	ENSP00000512084.1:p.Arg696=
ENST00000695654.1:c.3202C>A	ENSP00000512085.1:p.Arg1068=
ENST00000695689.1:c.148C>A	ENSP00000512101.1:n.148C>A
ENST00000695690.1:n.368C>A
ENST00000695691.1:n.368C>A
ENST00000245907.11:c.4177C>A MANE Select	ENSP00000245907.4:p.Arg1393=
ENST00000245907.10:c.4177C>A	ENSP00000245907.4:p.Arg1393=
ENST00000596548.1:c.298C>A	ENSP00000469744.1:p.Arg100=
ENST00000599899.5:n.1136C>A
ENST00000601008.1:c.242-4267C>A	ENSP00000471384.1:n.242-4267C>A
NM_000064.3:c.4177C>A	NP_000055.2:p.Arg1393=
NM_000064.4:c.4177C>A MANE Select	NP_000055.2:p.Arg1393=