Canonical Allele Identifier: CA403633566

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697562C>A (hg19) ; chr19:g.6697551C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697551C>A , CM000681.2:g.6697551C>A	GRCh38
NC_000019.9:g.6697562C>A , CM000681.1:g.6697562C>A	GRCh37
NC_000019.8:g.6648562C>A	NCBI36
NG_009557.1:g.28101G>T , LRG_27:g.28101G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.937G>T
ENST00000695652.1:c.2466G>T	ENSP00000512083.1:p.Arg822Ser
ENST00000695653.1:c.498G>T	ENSP00000512084.1:p.Arg166Ser
ENST00000695654.1:c.1713G>T	ENSP00000512085.1:p.Arg571Ser
ENST00000695655.1:c.1530G>T	ENSP00000512086.1:n.1530G>T
ENST00000695692.1:n.1953G>T
ENST00000245907.11:c.2589G>T MANE Select	ENSP00000245907.4:p.Arg863Ser
ENST00000245907.10:c.2589G>T	ENSP00000245907.4:p.Arg863Ser
ENST00000594005.1:n.165G>T
NM_000064.3:c.2589G>T	NP_000055.2:p.Arg863Ser
NM_000064.4:c.2589G>T MANE Select	NP_000055.2:p.Arg863Ser