Canonical Allele Identifier: CA403633266

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697512C>T (hg19) ; chr19:g.6697501C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697501C>T , CM000681.2:g.6697501C>T	GRCh38
NC_000019.9:g.6697512C>T , CM000681.1:g.6697512C>T	GRCh37
NC_000019.8:g.6648512C>T	NCBI36
NG_009557.1:g.28151G>A , LRG_27:g.28151G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.987G>A
ENST00000695652.1:c.2516G>A	ENSP00000512083.1:p.Arg839Lys
ENST00000695653.1:c.548G>A	ENSP00000512084.1:p.Arg183Lys
ENST00000695654.1:c.1763G>A	ENSP00000512085.1:p.Arg588Lys
ENST00000695655.1:c.1580G>A	ENSP00000512086.1:n.1580G>A
ENST00000695692.1:n.2003G>A
ENST00000245907.11:c.2639G>A MANE Select	ENSP00000245907.4:p.Arg880Lys
ENST00000245907.10:c.2639G>A	ENSP00000245907.4:p.Arg880Lys
ENST00000594005.1:n.215G>A
NM_000064.3:c.2639G>A	NP_000055.2:p.Arg880Lys
NM_000064.4:c.2639G>A MANE Select	NP_000055.2:p.Arg880Lys