Canonical Allele Identifier: CA2320551906
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682863A= , CM000681.2:g.6682863A= GRCh38
NC_000019.9:g.6682874A= , CM000681.1:g.6682874A= GRCh37
NC_000019.8:g.6633874A= NCBI36
NG_009557.1:g.42789T= , LRG_27:g.42789T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2521-634T=
ENST00000695653.1:c.2082-634T= ENSP00000512084.1:n.2082-634T=
ENST00000695654.1:c.3198-634T= ENSP00000512085.1:n.3198-634T=
ENST00000695689.1:c.84-197T= ENSP00000512101.1:n.84-197T=
ENST00000695690.1:n.364-634T=
ENST00000695691.1:n.364-634T=
ENST00000245907.11:c.4173-634T= MANE Select ENSP00000245907.4:n.4173-634T=
ENST00000245907.10:c.4173-634T= ENSP00000245907.4:n.4173-634T=
ENST00000596548.1:c.294-634T= ENSP00000469744.1:n.294-634T=
ENST00000599899.5:n.498T=
ENST00000601008.1:c.241+3883T= ENSP00000471384.1:n.241+3883T=
NM_000064.3:c.4173-634T= NP_000055.2:n.4173-634T=
NM_000064.4:c.4173-634T= MANE Select NP_000055.2:n.4173-634T=