Canonical Allele Identifier: CA2581367882
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6696586G>C , CM000681.2:g.6696586G>C GRCh38
NC_000019.9:g.6696597G>C , CM000681.1:g.6696597G>C GRCh37
NC_000019.8:g.6647597G>C NCBI36
NG_009557.1:g.29066C>G , LRG_27:g.29066C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.1211+7C>G
ENST00000695652.1:c.2740+7C>G ENSP00000512083.1:n.2740+7C>G
ENST00000695653.1:c.772+7C>G ENSP00000512084.1:n.772+7C>G
ENST00000695654.1:c.1987+7C>G ENSP00000512085.1:n.1987+7C>G
ENST00000695655.1:c.1804+7C>G ENSP00000512086.1:n.1804+7C>G
ENST00000695692.1:n.2227+7C>G
ENST00000245907.11:c.2863+7C>G MANE Select ENSP00000245907.4:n.2863+7C>G
ENST00000245907.10:c.2863+7C>G ENSP00000245907.4:n.2863+7C>G
NM_000064.3:c.2863+7C>G NP_000055.2:n.2863+7C>G
NM_000064.4:c.2863+7C>G MANE Select NP_000055.2:n.2863+7C>G
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