Canonical Allele Identifier: CA403633966

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697730A>C (hg19) ; chr19:g.6697719A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697719A>C , CM000681.2:g.6697719A>C	GRCh38
NC_000019.9:g.6697730A>C , CM000681.1:g.6697730A>C	GRCh37
NC_000019.8:g.6648730A>C	NCBI36
NG_009557.1:g.27933T>G , LRG_27:g.27933T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.864T>G
ENST00000695652.1:c.2393T>G	ENSP00000512083.1:p.Val798Gly
ENST00000695653.1:c.425T>G	ENSP00000512084.1:p.Val142Gly
ENST00000695654.1:c.1640T>G	ENSP00000512085.1:p.Val547Gly
ENST00000695655.1:c.1457T>G	ENSP00000512086.1:n.1457T>G
ENST00000695692.1:n.1880T>G
ENST00000245907.11:c.2516T>G MANE Select	ENSP00000245907.4:p.Val839Gly
ENST00000245907.10:c.2516T>G	ENSP00000245907.4:p.Val839Gly
ENST00000602053.1:n.564T>G
NM_000064.3:c.2516T>G	NP_000055.2:p.Val839Gly
NM_000064.4:c.2516T>G MANE Select	NP_000055.2:p.Val839Gly