Canonical Allele Identifier: CA2587878474
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713693del , CM000681.2:g.6713693del GRCh38
NC_000019.9:g.6713704del , CM000681.1:g.6713704del GRCh37
NC_000019.8:g.6664704del NCBI36
NG_009557.1:g.11964del , LRG_27:g.11964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-179del ENSP00000512083.1:n.651-179del
ENST00000245907.11:c.774-179del MANE Select ENSP00000245907.4:n.774-179del
ENST00000245907.10:c.774-179del ENSP00000245907.4:n.774-179del
ENST00000595577.1:n.278-179del
ENST00000597442.5:n.23+78del
NM_000064.3:c.774-179del NP_000055.2:n.774-179del
NM_000064.4:c.774-179del MANE Select NP_000055.2:n.774-179del