Canonical Allele Identifier: CA505192591

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697762G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697751G>A , CM000681.2:g.6697751G>A	GRCh38
NC_000019.9:g.6697762G>A , CM000681.1:g.6697762G>A	GRCh37
NC_000019.8:g.6648762G>A	NCBI36
NG_009557.1:g.27901C>T , LRG_27:g.27901C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.832C>T
ENST00000695652.1:c.2361C>T	ENSP00000512083.1:p.Asp787=
ENST00000695653.1:c.393C>T	ENSP00000512084.1:p.Asp131=
ENST00000695654.1:c.1608C>T	ENSP00000512085.1:p.Asp536=
ENST00000695655.1:c.1425C>T	ENSP00000512086.1:n.1425C>T
ENST00000695692.1:n.1848C>T
ENST00000245907.11:c.2484C>T MANE Select	ENSP00000245907.4:p.Asp828=
ENST00000245907.10:c.2484C>T	ENSP00000245907.4:p.Asp828=
ENST00000602053.1:n.532C>T
NM_000064.3:c.2484C>T	NP_000055.2:p.Asp828=
NM_000064.4:c.2484C>T MANE Select	NP_000055.2:p.Asp828=