Canonical Allele Identifier: CA2320557787
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599507703
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6694898C>T , CM000681.2:g.6694898C>T GRCh38
NC_000019.9:g.6694909C>T , CM000681.1:g.6694909C>T GRCh37
NC_000019.8:g.6645909C>T NCBI36
NG_009557.1:g.30754G>A , LRG_27:g.30754G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.1299-264G>A
ENST00000695652.1:c.2828-264G>A ENSP00000512083.1:n.2828-264G>A
ENST00000695653.1:c.860-264G>A ENSP00000512084.1:n.860-264G>A
ENST00000695654.1:c.2075-264G>A ENSP00000512085.1:n.2075-264G>A
ENST00000695655.1:c.1892-264G>A ENSP00000512086.1:n.1892-264G>A
ENST00000695692.1:n.2315-264G>A
ENST00000245907.11:c.2951-264G>A MANE Select ENSP00000245907.4:n.2951-264G>A
ENST00000245907.10:c.2951-264G>A ENSP00000245907.4:n.2951-264G>A
NM_000064.3:c.2951-264G>A NP_000055.2:n.2951-264G>A
NM_000064.4:c.2951-264G>A MANE Select NP_000055.2:n.2951-264G>A
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