Canonical Allele Identifier: CA304774831

Gene: C3

Linked Data

• dbSNP Id: rs201234298
• MyVariant Identifiers: chr19:g.6684847T>C (hg19) ; chr19:g.6684836T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684836T>C , CM000681.2:g.6684836T>C	GRCh38
NC_000019.9:g.6684847T>C , CM000681.1:g.6684847T>C	GRCh37
NC_000019.8:g.6635847T>C	NCBI36
NG_009557.1:g.40816A>G , LRG_27:g.40816A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2318-2A>G
ENST00000695653.1:c.1879-2A>G	ENSP00000512084.1:n.1879-2A>G
ENST00000695654.1:c.2995-2A>G	ENSP00000512085.1:n.2995-2A>G
ENST00000695690.1:n.161-2A>G
ENST00000695691.1:n.161-2A>G
ENST00000245907.11:c.3970-2A>G MANE Select	ENSP00000245907.4:n.3970-2A>G
ENST00000245907.10:c.3970-2A>G	ENSP00000245907.4:n.3970-2A>G
ENST00000596238.1:n.413-2A>G
ENST00000596548.1:c.52-2A>G	ENSP00000469744.1:n.52-2A>G
ENST00000601008.1:c.241+1910A>G	ENSP00000471384.1:n.241+1910A>G
NM_000064.3:c.3970-2A>G	NP_000055.2:n.3970-2A>G
NM_000064.4:c.3970-2A>G MANE Select	NP_000055.2:n.3970-2A>G