Canonical Allele Identifier: CA993075778
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1967948255
gnomAD v3: 19-6712836-GA-G
gnomAD v4: 19-6712836-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6712837del , CM000681.2:g.6712837del GRCh38
NC_000019.9:g.6712848del , CM000681.1:g.6712848del GRCh37
NC_000019.8:g.6663848del NCBI36
NG_009557.1:g.12815del , LRG_27:g.12815del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.881-214del ENSP00000512083.1:n.881-214del
ENST00000695654.1:c.128-214del ENSP00000512085.1:n.128-214del
ENST00000695692.1:n.328-174del
ENST00000245907.11:c.1004-214del MANE Select ENSP00000245907.4:n.1004-214del
ENST00000245907.10:c.1004-214del ENSP00000245907.4:n.1004-214del
ENST00000594270.5:n.128-235del
ENST00000595577.1:n.508-214del
ENST00000597442.5:n.254-214del
NM_000064.3:c.1004-214del NP_000055.2:n.1004-214del
NM_000064.4:c.1004-214del MANE Select NP_000055.2:n.1004-214del
Search 100 bp 5'
Search 100 bp 3'