Canonical Allele Identifier: CA505119966

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679167C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679156C>T , CM000681.2:g.6679156C>T	GRCh38
NC_000019.9:g.6679167C>T , CM000681.1:g.6679167C>T	GRCh37
NC_000019.8:g.6630167C>T	NCBI36
NG_009557.1:g.46496G>A , LRG_27:g.46496G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2947G>A
ENST00000695653.1:c.2508G>A	ENSP00000512084.1:p.Leu836=
ENST00000695654.1:c.3624G>A	ENSP00000512085.1:p.Leu1208=
ENST00000695689.1:c.570G>A	ENSP00000512101.1:n.570G>A
ENST00000695690.1:n.1664G>A
ENST00000695691.1:n.1460G>A
ENST00000245907.11:c.4599G>A MANE Select	ENSP00000245907.4:p.Leu1533=
ENST00000245907.10:c.4599G>A	ENSP00000245907.4:p.Leu1533=
ENST00000599668.1:n.219G>A
ENST00000599899.5:n.1558G>A
ENST00000601008.1:c.242-1198G>A	ENSP00000471384.1:n.242-1198G>A
ENST00000602229.1:c.46G>A
NM_000064.3:c.4599G>A	NP_000055.2:p.Leu1533=
NM_000064.4:c.4599G>A MANE Select	NP_000055.2:p.Leu1533=