Canonical Allele Identifier: CA505192372

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697513T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697502T>G , CM000681.2:g.6697502T>G	GRCh38
NC_000019.9:g.6697513T>G , CM000681.1:g.6697513T>G	GRCh37
NC_000019.8:g.6648513T>G	NCBI36
NG_009557.1:g.28150A>C , LRG_27:g.28150A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.986A>C
ENST00000695652.1:c.2515A>C	ENSP00000512083.1:p.Arg839=
ENST00000695653.1:c.547A>C	ENSP00000512084.1:p.Arg183=
ENST00000695654.1:c.1762A>C	ENSP00000512085.1:p.Arg588=
ENST00000695655.1:c.1579A>C	ENSP00000512086.1:n.1579A>C
ENST00000695692.1:n.2002A>C
ENST00000245907.11:c.2638A>C MANE Select	ENSP00000245907.4:p.Arg880=
ENST00000245907.10:c.2638A>C	ENSP00000245907.4:p.Arg880=
ENST00000594005.1:n.214A>C
NM_000064.3:c.2638A>C	NP_000055.2:p.Arg880=
NM_000064.4:c.2638A>C MANE Select	NP_000055.2:p.Arg880=