Canonical Allele Identifier: CA403633978

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697735G>C (hg19) ; chr19:g.6697724G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697724G>C , CM000681.2:g.6697724G>C	GRCh38
NC_000019.9:g.6697735G>C , CM000681.1:g.6697735G>C	GRCh37
NC_000019.8:g.6648735G>C	NCBI36
NG_009557.1:g.27928C>G , LRG_27:g.27928C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.859C>G
ENST00000695652.1:c.2388C>G	ENSP00000512083.1:p.Tyr796Ter
ENST00000695653.1:c.420C>G	ENSP00000512084.1:p.Tyr140Ter
ENST00000695654.1:c.1635C>G	ENSP00000512085.1:p.Tyr545Ter
ENST00000695655.1:c.1452C>G	ENSP00000512086.1:n.1452C>G
ENST00000695692.1:n.1875C>G
ENST00000245907.11:c.2511C>G MANE Select	ENSP00000245907.4:p.Tyr837Ter
ENST00000245907.10:c.2511C>G	ENSP00000245907.4:p.Tyr837Ter
ENST00000602053.1:n.559C>G
NM_000064.3:c.2511C>G	NP_000055.2:p.Tyr837Ter
NM_000064.4:c.2511C>G MANE Select	NP_000055.2:p.Tyr837Ter