Canonical Allele Identifier: CA505192500

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697723T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697712T>C , CM000681.2:g.6697712T>C	GRCh38
NC_000019.9:g.6697723T>C , CM000681.1:g.6697723T>C	GRCh37
NC_000019.8:g.6648723T>C	NCBI36
NG_009557.1:g.27940A>G , LRG_27:g.27940A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.871A>G
ENST00000695652.1:c.2400A>G	ENSP00000512083.1:p.Arg800=
ENST00000695653.1:c.432A>G	ENSP00000512084.1:p.Arg144=
ENST00000695654.1:c.1647A>G	ENSP00000512085.1:p.Arg549=
ENST00000695655.1:c.1464A>G	ENSP00000512086.1:n.1464A>G
ENST00000695692.1:n.1887A>G
ENST00000245907.11:c.2523A>G MANE Select	ENSP00000245907.4:p.Arg841=
ENST00000245907.10:c.2523A>G	ENSP00000245907.4:p.Arg841=
ENST00000594005.1:n.4A>G
ENST00000602053.1:n.571A>G
NM_000064.3:c.2523A>G	NP_000055.2:p.Arg841=
NM_000064.4:c.2523A>G MANE Select	NP_000055.2:p.Arg841=