Canonical Allele Identifier: CA2320551548
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6681982C= , CM000681.2:g.6681982C= GRCh38
NC_000019.9:g.6681993C= , CM000681.1:g.6681993C= GRCh37
NC_000019.8:g.6632993C= NCBI36
NG_009557.1:g.43670G= , LRG_27:g.43670G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2657G=
ENST00000695653.1:c.2218G= ENSP00000512084.1:p.Ala740=
ENST00000695654.1:c.3334G= ENSP00000512085.1:p.Ala1112=
ENST00000695689.1:c.280G= ENSP00000512101.1:n.280G=
ENST00000695690.1:n.500G=
ENST00000695691.1:n.500G=
ENST00000245907.11:c.4309G= MANE Select ENSP00000245907.4:p.Ala1437=
ENST00000245907.10:c.4309G= ENSP00000245907.4:p.Ala1437=
ENST00000596548.1:c.430G= ENSP00000469744.1:p.Ala144=
ENST00000599899.5:n.1268G=
ENST00000601008.1:c.242-4024G= ENSP00000471384.1:n.242-4024G=
NM_000064.3:c.4309G= NP_000055.2:p.Ala1437=
NM_000064.4:c.4309G= MANE Select NP_000055.2:p.Ala1437=