Canonical Allele Identifier: CA505123572

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685134G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685123G>T , CM000681.2:g.6685123G>T	GRCh38
NC_000019.9:g.6685134G>T , CM000681.1:g.6685134G>T	GRCh37
NC_000019.8:g.6636134G>T	NCBI36
NG_009557.1:g.40529C>A , LRG_27:g.40529C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2182C>A
ENST00000695653.1:c.1743C>A	ENSP00000512084.1:p.Ala581=
ENST00000695654.1:c.2859C>A	ENSP00000512085.1:p.Ala953=
ENST00000695690.1:n.25C>A
ENST00000695691.1:n.25C>A
ENST00000245907.11:c.3834C>A MANE Select	ENSP00000245907.4:p.Ala1278=
ENST00000245907.10:c.3834C>A	ENSP00000245907.4:p.Ala1278=
ENST00000596238.1:n.277C>A
ENST00000601008.1:c.241+1623C>A	ENSP00000471384.1:n.241+1623C>A
NM_000064.3:c.3834C>A	NP_000055.2:p.Ala1278=
NM_000064.4:c.3834C>A MANE Select	NP_000055.2:p.Ala1278=