Canonical Allele Identifier: CA2320568282
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599525388
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713882C>G , CM000681.2:g.6713882C>G GRCh38
NC_000019.9:g.6713893C>G , CM000681.1:g.6713893C>G GRCh37
NC_000019.8:g.6664893C>G NCBI36
NG_009557.1:g.11770G>C , LRG_27:g.11770G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+110G>C ENSP00000512083.1:n.650+110G>C
ENST00000245907.11:c.773+110G>C MANE Select ENSP00000245907.4:n.773+110G>C
ENST00000245907.10:c.773+110G>C ENSP00000245907.4:n.773+110G>C
ENST00000595577.1:n.277+110G>C
NM_000064.3:c.773+110G>C NP_000055.2:n.773+110G>C
NM_000064.4:c.773+110G>C MANE Select NP_000055.2:n.773+110G>C
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