Canonical Allele Identifier: CA505122282

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682000C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681989C>T , CM000681.2:g.6681989C>T	GRCh38
NC_000019.9:g.6682000C>T , CM000681.1:g.6682000C>T	GRCh37
NC_000019.8:g.6633000C>T	NCBI36
NG_009557.1:g.43663G>A , LRG_27:g.43663G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2650G>A
ENST00000695653.1:c.2211G>A	ENSP00000512084.1:p.Leu737=
ENST00000695654.1:c.3327G>A	ENSP00000512085.1:p.Leu1109=
ENST00000695689.1:c.273G>A	ENSP00000512101.1:n.273G>A
ENST00000695690.1:n.493G>A
ENST00000695691.1:n.493G>A
ENST00000245907.11:c.4302G>A MANE Select	ENSP00000245907.4:p.Leu1434=
ENST00000245907.10:c.4302G>A	ENSP00000245907.4:p.Leu1434=
ENST00000596548.1:c.423G>A	ENSP00000469744.1:p.Leu141=
ENST00000599899.5:n.1261G>A
ENST00000601008.1:c.242-4031G>A	ENSP00000471384.1:n.242-4031G>A
NM_000064.3:c.4302G>A	NP_000055.2:p.Leu1434=
NM_000064.4:c.4302G>A MANE Select	NP_000055.2:p.Leu1434=