Canonical Allele Identifier: CA403632493

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697362T>C (hg19) ; chr19:g.6697351T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697351T>C , CM000681.2:g.6697351T>C	GRCh38
NC_000019.9:g.6697362T>C , CM000681.1:g.6697362T>C	GRCh37
NC_000019.8:g.6648362T>C	NCBI36
NG_009557.1:g.28301A>G , LRG_27:g.28301A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1137A>G
ENST00000695652.1:c.2666A>G	ENSP00000512083.1:p.Lys889Arg
ENST00000695653.1:c.698A>G	ENSP00000512084.1:p.Lys233Arg
ENST00000695654.1:c.1913A>G	ENSP00000512085.1:p.Lys638Arg
ENST00000695655.1:c.1730A>G	ENSP00000512086.1:n.1730A>G
ENST00000695692.1:n.2153A>G
ENST00000245907.11:c.2789A>G MANE Select	ENSP00000245907.4:p.Lys930Arg
ENST00000245907.10:c.2789A>G	ENSP00000245907.4:p.Lys930Arg
ENST00000594005.1:n.365A>G
NM_000064.3:c.2789A>G	NP_000055.2:p.Lys930Arg
NM_000064.4:c.2789A>G MANE Select	NP_000055.2:p.Lys930Arg