Canonical Allele Identifier: CA2320550365
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679308C= , CM000681.2:g.6679308C= GRCh38
NC_000019.9:g.6679319C= , CM000681.1:g.6679319C= GRCh37
NC_000019.8:g.6630319C= NCBI36
NG_009557.1:g.46344G= , LRG_27:g.46344G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2895-100G=
ENST00000695653.1:c.2456-100G= ENSP00000512084.1:n.2456-100G=
ENST00000695654.1:c.3572-100G= ENSP00000512085.1:n.3572-100G=
ENST00000695689.1:c.518-100G= ENSP00000512101.1:n.518-100G=
ENST00000695690.1:n.1612-100G=
ENST00000695691.1:n.1408-100G=
ENST00000245907.11:c.4547-100G= MANE Select ENSP00000245907.4:n.4547-100G=
ENST00000245907.10:c.4547-100G= ENSP00000245907.4:n.4547-100G=
ENST00000599668.1:n.166+74G=
ENST00000599899.5:n.1506-100G=
ENST00000601008.1:c.242-1350G= ENSP00000471384.1:n.242-1350G=
NM_000064.3:c.4547-100G= NP_000055.2:n.4547-100G=
NM_000064.4:c.4547-100G= MANE Select NP_000055.2:n.4547-100G=