Canonical Allele Identifier: CA2320567955
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713512A= , CM000681.2:g.6713512A= GRCh38
NC_000019.9:g.6713523A= , CM000681.1:g.6713523A= GRCh37
NC_000019.8:g.6664523A= NCBI36
NG_009557.1:g.12140T= , LRG_27:g.12140T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-3T= ENSP00000512083.1:n.651-3T=
ENST00000695692.1:n.95T=
ENST00000245907.11:c.774-3T= MANE Select ENSP00000245907.4:n.774-3T=
ENST00000245907.10:c.774-3T= ENSP00000245907.4:n.774-3T=
ENST00000595577.1:n.278-3T=
ENST00000597442.5:n.24-3T=
NM_000064.3:c.774-3T= NP_000055.2:n.774-3T=
NM_000064.4:c.774-3T= MANE Select NP_000055.2:n.774-3T=
Search 100 bp 5'
Search 100 bp 3'