Canonical Allele Identifier: CA2320565817
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1967858904
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709542C>T , CM000681.2:g.6709542C>T GRCh38
NC_000019.9:g.6709553C>T , CM000681.1:g.6709553C>T GRCh37
NC_000019.8:g.6660553C>T NCBI36
NG_009557.1:g.16110G>A , LRG_27:g.16110G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1722+142G>A ENSP00000512083.1:n.1722+142G>A
ENST00000695654.1:c.969+142G>A ENSP00000512085.1:n.969+142G>A
ENST00000695655.1:c.786+142G>A ENSP00000512086.1:n.786+142G>A
ENST00000695692.1:n.1209+142G>A
ENST00000245907.11:c.1845+142G>A MANE Select ENSP00000245907.4:n.1845+142G>A
ENST00000245907.10:c.1845+142G>A ENSP00000245907.4:n.1845+142G>A
NM_000064.3:c.1845+142G>A NP_000055.2:n.1845+142G>A
NM_000064.4:c.1845+142G>A MANE Select NP_000055.2:n.1845+142G>A
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