Canonical Allele Identifier: CA505122426

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682222A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682211A>G , CM000681.2:g.6682211A>G	GRCh38
NC_000019.9:g.6682222A>G , CM000681.1:g.6682222A>G	GRCh37
NC_000019.8:g.6633222A>G	NCBI36
NG_009557.1:g.43441T>C , LRG_27:g.43441T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2539T>C
ENST00000695653.1:c.2100T>C	ENSP00000512084.1:p.Asp700=
ENST00000695654.1:c.3216T>C	ENSP00000512085.1:p.Asp1072=
ENST00000695689.1:c.162T>C	ENSP00000512101.1:n.162T>C
ENST00000695690.1:n.382T>C
ENST00000695691.1:n.382T>C
ENST00000245907.11:c.4191T>C MANE Select	ENSP00000245907.4:p.Asp1397=
ENST00000245907.10:c.4191T>C	ENSP00000245907.4:p.Asp1397=
ENST00000596548.1:c.312T>C	ENSP00000469744.1:p.Asp104=
ENST00000599899.5:n.1150T>C
ENST00000601008.1:c.242-4253T>C	ENSP00000471384.1:n.242-4253T>C
NM_000064.3:c.4191T>C	NP_000055.2:p.Asp1397=
NM_000064.4:c.4191T>C MANE Select	NP_000055.2:p.Asp1397=