Canonical Allele Identifier: CA2320568664
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1967993792
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714620G>C , CM000681.2:g.6714620G>C GRCh38
NC_000019.9:g.6714631G>C , CM000681.1:g.6714631G>C GRCh37
NC_000019.8:g.6665631G>C NCBI36
NG_009557.1:g.11032C>G , LRG_27:g.11032C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.382-174C>G ENSP00000512083.1:n.382-174C>G
ENST00000245907.11:c.505-174C>G MANE Select ENSP00000245907.4:n.505-174C>G
ENST00000245907.10:c.505-174C>G ENSP00000245907.4:n.505-174C>G
NM_000064.3:c.505-174C>G NP_000055.2:n.505-174C>G
NM_000064.4:c.505-174C>G MANE Select NP_000055.2:n.505-174C>G
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