Canonical Allele Identifier: CA2571948887
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6694946T>C , CM000681.2:g.6694946T>C GRCh38
NC_000019.9:g.6694957T>C , CM000681.1:g.6694957T>C GRCh37
NC_000019.8:g.6645957T>C NCBI36
NG_009557.1:g.30706A>G , LRG_27:g.30706A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.1299-312A>G
ENST00000695652.1:c.2828-312A>G ENSP00000512083.1:n.2828-312A>G
ENST00000695653.1:c.860-312A>G ENSP00000512084.1:n.860-312A>G
ENST00000695654.1:c.2075-312A>G ENSP00000512085.1:n.2075-312A>G
ENST00000695655.1:c.1892-312A>G ENSP00000512086.1:n.1892-312A>G
ENST00000695692.1:n.2315-312A>G
ENST00000245907.11:c.2951-312A>G MANE Select ENSP00000245907.4:n.2951-312A>G
ENST00000245907.10:c.2951-312A>G ENSP00000245907.4:n.2951-312A>G
NM_000064.3:c.2951-312A>G NP_000055.2:n.2951-312A>G
NM_000064.4:c.2951-312A>G MANE Select NP_000055.2:n.2951-312A>G
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