Canonical Allele Identifier: CA505192352

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697535G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697524G>A , CM000681.2:g.6697524G>A	GRCh38
NC_000019.9:g.6697535G>A , CM000681.1:g.6697535G>A	GRCh37
NC_000019.8:g.6648535G>A	NCBI36
NG_009557.1:g.28128C>T , LRG_27:g.28128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.964C>T
ENST00000695652.1:c.2493C>T	ENSP00000512083.1:p.Phe831=
ENST00000695653.1:c.525C>T	ENSP00000512084.1:p.Phe175=
ENST00000695654.1:c.1740C>T	ENSP00000512085.1:p.Phe580=
ENST00000695655.1:c.1557C>T	ENSP00000512086.1:n.1557C>T
ENST00000695692.1:n.1980C>T
ENST00000245907.11:c.2616C>T MANE Select	ENSP00000245907.4:p.Phe872=
ENST00000245907.10:c.2616C>T	ENSP00000245907.4:p.Phe872=
ENST00000594005.1:n.192C>T
NM_000064.3:c.2616C>T	NP_000055.2:p.Phe872=
NM_000064.4:c.2616C>T MANE Select	NP_000055.2:p.Phe872=