Canonical Allele Identifier: CA2320557806
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6694944T= , CM000681.2:g.6694944T= GRCh38
NC_000019.9:g.6694955T= , CM000681.1:g.6694955T= GRCh37
NC_000019.8:g.6645955T= NCBI36
NG_009557.1:g.30708A= , LRG_27:g.30708A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.1299-310A=
ENST00000695652.1:c.2828-310A= ENSP00000512083.1:n.2828-310A=
ENST00000695653.1:c.860-310A= ENSP00000512084.1:n.860-310A=
ENST00000695654.1:c.2075-310A= ENSP00000512085.1:n.2075-310A=
ENST00000695655.1:c.1892-310A= ENSP00000512086.1:n.1892-310A=
ENST00000695692.1:n.2315-310A=
ENST00000245907.11:c.2951-310A= MANE Select ENSP00000245907.4:n.2951-310A=
ENST00000245907.10:c.2951-310A= ENSP00000245907.4:n.2951-310A=
NM_000064.3:c.2951-310A= NP_000055.2:n.2951-310A=
NM_000064.4:c.2951-310A= MANE Select NP_000055.2:n.2951-310A=