Canonical Allele Identifier: CA403632640

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697387T>A (hg19) ; chr19:g.6697376T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697376T>A , CM000681.2:g.6697376T>A	GRCh38
NC_000019.9:g.6697387T>A , CM000681.1:g.6697387T>A	GRCh37
NC_000019.8:g.6648387T>A	NCBI36
NG_009557.1:g.28276A>T , LRG_27:g.28276A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1112A>T
ENST00000695652.1:c.2641A>T	ENSP00000512083.1:p.Ser881Cys
ENST00000695653.1:c.673A>T	ENSP00000512084.1:p.Ser225Cys
ENST00000695654.1:c.1888A>T	ENSP00000512085.1:p.Ser630Cys
ENST00000695655.1:c.1705A>T	ENSP00000512086.1:n.1705A>T
ENST00000695692.1:n.2128A>T
ENST00000245907.11:c.2764A>T MANE Select	ENSP00000245907.4:p.Ser922Cys
ENST00000245907.10:c.2764A>T	ENSP00000245907.4:p.Ser922Cys
ENST00000594005.1:n.340A>T
NM_000064.3:c.2764A>T	NP_000055.2:p.Ser922Cys
NM_000064.4:c.2764A>T MANE Select	NP_000055.2:p.Ser922Cys