Canonical Allele Identifier: CA9128245

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6678175G>A , CM000681.2:g.6678175G>A	GRCh38
NC_000019.9:g.6678186G>A , CM000681.1:g.6678186G>A	GRCh37
NC_000019.8:g.6629186G>A	NCBI36
NG_009557.1:g.47477C>T , LRG_27:g.47477C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.4827C>T MANE Select	NP_000055.2:p.Ser1609=
ENST00000245907.11:c.4827C>T MANE Select	ENSP00000245907.4:p.Ser1609=
NM_000064.3:c.4827C>T	NP_000055.2:p.Ser1609=
ENST00000245907.10:c.4827C>T	ENSP00000245907.4:p.Ser1609=
ENST00000599668.1:n.447C>T
ENST00000599899.5:n.1786C>T
ENST00000601008.1:c.242-217C>T	ENSP00000471384.1:n.242-217C>T
ENST00000601475.1:n.156C>T
ENST00000602229.1:c.274C>T
ENST00000695651.1:n.3175C>T
ENST00000695653.1:c.2736C>T	ENSP00000512084.1:p.Ser912=
ENST00000695654.1:c.3852C>T	ENSP00000512085.1:p.Ser1284=
ENST00000695689.1:c.798C>T	ENSP00000512101.1:n.798C>T
ENST00000695690.1:n.1892C>T
ENST00000695691.1:n.1688C>T