Canonical Allele Identifier: CA505192345

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697490G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697479G>T , CM000681.2:g.6697479G>T	GRCh38
NC_000019.9:g.6697490G>T , CM000681.1:g.6697490G>T	GRCh37
NC_000019.8:g.6648490G>T	NCBI36
NG_009557.1:g.28173C>A , LRG_27:g.28173C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1009C>A
ENST00000695652.1:c.2538C>A	ENSP00000512083.1:p.Thr846=
ENST00000695653.1:c.570C>A	ENSP00000512084.1:p.Thr190=
ENST00000695654.1:c.1785C>A	ENSP00000512085.1:p.Thr595=
ENST00000695655.1:c.1602C>A	ENSP00000512086.1:n.1602C>A
ENST00000695692.1:n.2025C>A
ENST00000245907.11:c.2661C>A MANE Select	ENSP00000245907.4:p.Thr887=
ENST00000245907.10:c.2661C>A	ENSP00000245907.4:p.Thr887=
ENST00000594005.1:n.237C>A
NM_000064.3:c.2661C>A	NP_000055.2:p.Thr887=
NM_000064.4:c.2661C>A MANE Select	NP_000055.2:p.Thr887=