Canonical Allele Identifier: CA403633739

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697676T>G (hg19) ; chr19:g.6697665T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697665T>G , CM000681.2:g.6697665T>G	GRCh38
NC_000019.9:g.6697676T>G , CM000681.1:g.6697676T>G	GRCh37
NC_000019.8:g.6648676T>G	NCBI36
NG_009557.1:g.27987A>C , LRG_27:g.27987A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.918A>C
ENST00000695652.1:c.2447A>C	ENSP00000512083.1:p.Asn816Thr
ENST00000695653.1:c.479A>C	ENSP00000512084.1:p.Asn160Thr
ENST00000695654.1:c.1694A>C	ENSP00000512085.1:p.Asn565Thr
ENST00000695655.1:c.1511A>C	ENSP00000512086.1:n.1511A>C
ENST00000695692.1:n.1934A>C
ENST00000245907.11:c.2570A>C MANE Select	ENSP00000245907.4:p.Asn857Thr
ENST00000245907.10:c.2570A>C	ENSP00000245907.4:p.Asn857Thr
ENST00000594005.1:n.51A>C
ENST00000602053.1:n.618A>C
NM_000064.3:c.2570A>C	NP_000055.2:p.Asn857Thr
NM_000064.4:c.2570A>C MANE Select	NP_000055.2:p.Asn857Thr