Canonical Allele Identifier: CA9128539

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684654G>A , CM000681.2:g.6684654G>A	GRCh38
NC_000019.9:g.6684665G>A , CM000681.1:g.6684665G>A	GRCh37
NC_000019.8:g.6635665G>A	NCBI36
NG_009557.1:g.40998C>T , LRG_27:g.40998C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.4030-4C>T MANE Select	NP_000055.2:n.4030-4C>T
ENST00000245907.11:c.4030-4C>T MANE Select	ENSP00000245907.4:n.4030-4C>T
NM_000064.3:c.4030-4C>T	NP_000055.2:n.4030-4C>T
ENST00000245907.10:c.4030-4C>T	ENSP00000245907.4:n.4030-4C>T
ENST00000596238.1:n.473-4C>T
ENST00000596548.1:c.112-4C>T	ENSP00000469744.1:n.112-4C>T
ENST00000601008.1:c.241+2092C>T	ENSP00000471384.1:n.241+2092C>T
ENST00000695651.1:n.2378-4C>T
ENST00000695653.1:c.1939-4C>T	ENSP00000512084.1:n.1939-4C>T
ENST00000695654.1:c.3055-4C>T	ENSP00000512085.1:n.3055-4C>T
ENST00000695690.1:n.221-4C>T
ENST00000695691.1:n.221-4C>T