Canonical Allele Identifier: CA505120248
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6679431G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679420G>A , CM000681.2:g.6679420G>A GRCh38
NC_000019.9:g.6679431G>A , CM000681.1:g.6679431G>A GRCh37
NC_000019.8:g.6630431G>A NCBI36
NG_009557.1:g.46232C>T , LRG_27:g.46232C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2881C>T
ENST00000695653.1:c.2442C>T ENSP00000512084.1:p.Cys814=
ENST00000695654.1:c.3558C>T ENSP00000512085.1:p.Cys1186=
ENST00000695689.1:c.504C>T ENSP00000512101.1:n.504C>T
ENST00000695690.1:n.1598C>T
ENST00000695691.1:n.1394C>T
ENST00000245907.11:c.4533C>T MANE Select ENSP00000245907.4:p.Cys1511=
ENST00000245907.10:c.4533C>T ENSP00000245907.4:p.Cys1511=
ENST00000599668.1:n.128C>T
ENST00000599899.5:n.1492C>T
ENST00000601008.1:c.242-1462C>T ENSP00000471384.1:n.242-1462C>T
NM_000064.3:c.4533C>T NP_000055.2:p.Cys1511=
NM_000064.4:c.4533C>T MANE Select NP_000055.2:p.Cys1511=