Canonical Allele Identifier: CA403639153

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709700T>G (hg19) ; chr19:g.6709689T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709689T>G , CM000681.2:g.6709689T>G	GRCh38
NC_000019.9:g.6709700T>G , CM000681.1:g.6709700T>G	GRCh37
NC_000019.8:g.6660700T>G	NCBI36
NG_009557.1:g.15963A>C , LRG_27:g.15963A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1717A>C	ENSP00000512083.1:p.Ser573Arg
ENST00000695654.1:c.964A>C	ENSP00000512085.1:p.Ser322Arg
ENST00000695655.1:c.781A>C	ENSP00000512086.1:n.781A>C
ENST00000695692.1:n.1204A>C
ENST00000245907.11:c.1840A>C MANE Select	ENSP00000245907.4:p.Ser614Arg
ENST00000245907.10:c.1840A>C	ENSP00000245907.4:p.Ser614Arg
NM_000064.3:c.1840A>C	NP_000055.2:p.Ser614Arg
NM_000064.4:c.1840A>C MANE Select	NP_000055.2:p.Ser614Arg