Canonical Allele Identifier: CA403633939

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697718T>C (hg19) ; chr19:g.6697707T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697707T>C , CM000681.2:g.6697707T>C	GRCh38
NC_000019.9:g.6697718T>C , CM000681.1:g.6697718T>C	GRCh37
NC_000019.8:g.6648718T>C	NCBI36
NG_009557.1:g.27945A>G , LRG_27:g.27945A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.876A>G
ENST00000695652.1:c.2405A>G	ENSP00000512083.1:p.Glu802Gly
ENST00000695653.1:c.437A>G	ENSP00000512084.1:p.Glu146Gly
ENST00000695654.1:c.1652A>G	ENSP00000512085.1:p.Glu551Gly
ENST00000695655.1:c.1469A>G	ENSP00000512086.1:n.1469A>G
ENST00000695692.1:n.1892A>G
ENST00000245907.11:c.2528A>G MANE Select	ENSP00000245907.4:p.Glu843Gly
ENST00000245907.10:c.2528A>G	ENSP00000245907.4:p.Glu843Gly
ENST00000594005.1:n.9A>G
ENST00000602053.1:n.576A>G
NM_000064.3:c.2528A>G	NP_000055.2:p.Glu843Gly
NM_000064.4:c.2528A>G MANE Select	NP_000055.2:p.Glu843Gly