Canonical Allele Identifier: CA2320551896
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682848C= , CM000681.2:g.6682848C= GRCh38
NC_000019.9:g.6682859C= , CM000681.1:g.6682859C= GRCh37
NC_000019.8:g.6633859C= NCBI36
NG_009557.1:g.42804G= , LRG_27:g.42804G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2521-619G=
ENST00000695653.1:c.2082-619G= ENSP00000512084.1:n.2082-619G=
ENST00000695654.1:c.3198-619G= ENSP00000512085.1:n.3198-619G=
ENST00000695689.1:c.84-182G= ENSP00000512101.1:n.84-182G=
ENST00000695690.1:n.364-619G=
ENST00000695691.1:n.364-619G=
ENST00000245907.11:c.4173-619G= MANE Select ENSP00000245907.4:n.4173-619G=
ENST00000245907.10:c.4173-619G= ENSP00000245907.4:n.4173-619G=
ENST00000596548.1:c.294-619G= ENSP00000469744.1:n.294-619G=
ENST00000599899.5:n.513G=
ENST00000601008.1:c.241+3898G= ENSP00000471384.1:n.241+3898G=
NM_000064.3:c.4173-619G= NP_000055.2:n.4173-619G=
NM_000064.4:c.4173-619G= MANE Select NP_000055.2:n.4173-619G=