Canonical Allele Identifier: CA304783981

Gene: C3

Linked Data

• dbSNP Id: rs983997364
• MyVariant Identifiers: chr19:g.6694907A>C (hg19) ; chr19:g.6694896A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694896A>C , CM000681.2:g.6694896A>C	GRCh38
NC_000019.9:g.6694907A>C , CM000681.1:g.6694907A>C	GRCh37
NC_000019.8:g.6645907A>C	NCBI36
NG_009557.1:g.30756T>G , LRG_27:g.30756T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.1299-262T>G
ENST00000695652.1:c.2828-262T>G	ENSP00000512083.1:n.2828-262T>G
ENST00000695653.1:c.860-262T>G	ENSP00000512084.1:n.860-262T>G
ENST00000695654.1:c.2075-262T>G	ENSP00000512085.1:n.2075-262T>G
ENST00000695655.1:c.1892-262T>G	ENSP00000512086.1:n.1892-262T>G
ENST00000695692.1:n.2315-262T>G
ENST00000245907.11:c.2951-262T>G MANE Select	ENSP00000245907.4:n.2951-262T>G
ENST00000245907.10:c.2951-262T>G	ENSP00000245907.4:n.2951-262T>G
NM_000064.3:c.2951-262T>G	NP_000055.2:n.2951-262T>G
NM_000064.4:c.2951-262T>G MANE Select	NP_000055.2:n.2951-262T>G