Canonical Allele Identifier: CA403612838

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679486T>G (hg19) ; chr19:g.6679475T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679475T>G , CM000681.2:g.6679475T>G	GRCh38
NC_000019.9:g.6679486T>G , CM000681.1:g.6679486T>G	GRCh37
NC_000019.8:g.6630486T>G	NCBI36
NG_009557.1:g.46177A>C , LRG_27:g.46177A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2826A>C
ENST00000695653.1:c.2387A>C	ENSP00000512084.1:p.Tyr796Ser
ENST00000695654.1:c.3503A>C	ENSP00000512085.1:p.Tyr1168Ser
ENST00000695689.1:c.449A>C	ENSP00000512101.1:n.449A>C
ENST00000695690.1:n.1543A>C
ENST00000695691.1:n.1339A>C
ENST00000245907.11:c.4478A>C MANE Select	ENSP00000245907.4:p.Tyr1493Ser
ENST00000245907.10:c.4478A>C	ENSP00000245907.4:p.Tyr1493Ser
ENST00000599668.1:n.73A>C
ENST00000599899.5:n.1437A>C
ENST00000601008.1:c.242-1517A>C	ENSP00000471384.1:n.242-1517A>C
NM_000064.3:c.4478A>C	NP_000055.2:p.Tyr1493Ser
NM_000064.4:c.4478A>C MANE Select	NP_000055.2:p.Tyr1493Ser