Canonical Allele Identifier: CA403612752

Gene: C3

Linked Data

• dbSNP Id: rs1485072981
• MyVariant Identifiers: chr19:g.6679456T>C (hg19) ; chr19:g.6679445T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679445T>C , CM000681.2:g.6679445T>C	GRCh38
NC_000019.9:g.6679456T>C , CM000681.1:g.6679456T>C	GRCh37
NC_000019.8:g.6630456T>C	NCBI36
NG_009557.1:g.46207A>G , LRG_27:g.46207A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2856A>G
ENST00000695653.1:c.2417A>G	ENSP00000512084.1:p.Asn806Ser
ENST00000695654.1:c.3533A>G	ENSP00000512085.1:p.Asn1178Ser
ENST00000695689.1:c.479A>G	ENSP00000512101.1:n.479A>G
ENST00000695690.1:n.1573A>G
ENST00000695691.1:n.1369A>G
ENST00000245907.11:c.4508A>G MANE Select	ENSP00000245907.4:p.Asn1503Ser
ENST00000245907.10:c.4508A>G	ENSP00000245907.4:p.Asn1503Ser
ENST00000599668.1:n.103A>G
ENST00000599899.5:n.1467A>G
ENST00000601008.1:c.242-1487A>G	ENSP00000471384.1:n.242-1487A>G
NM_000064.3:c.4508A>G	NP_000055.2:p.Asn1503Ser
NM_000064.4:c.4508A>G MANE Select	NP_000055.2:p.Asn1503Ser