Canonical Allele Identifier: CA2320568002
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599525019
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713597A>T , CM000681.2:g.6713597A>T GRCh38
NC_000019.9:g.6713608A>T , CM000681.1:g.6713608A>T GRCh37
NC_000019.8:g.6664608A>T NCBI36
NG_009557.1:g.12055T>A , LRG_27:g.12055T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-88T>A ENSP00000512083.1:n.651-88T>A
ENST00000695692.1:n.10T>A
ENST00000245907.11:c.774-88T>A MANE Select ENSP00000245907.4:n.774-88T>A
ENST00000245907.10:c.774-88T>A ENSP00000245907.4:n.774-88T>A
ENST00000595577.1:n.278-88T>A
ENST00000597442.5:n.24-88T>A
NM_000064.3:c.774-88T>A NP_000055.2:n.774-88T>A
NM_000064.4:c.774-88T>A MANE Select NP_000055.2:n.774-88T>A
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