Canonical Allele Identifier: CA2320568065
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713671A= , CM000681.2:g.6713671A= GRCh38
NC_000019.9:g.6713682A= , CM000681.1:g.6713682A= GRCh37
NC_000019.8:g.6664682A= NCBI36
NG_009557.1:g.11981T= , LRG_27:g.11981T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-162T= ENSP00000512083.1:n.651-162T=
ENST00000245907.11:c.774-162T= MANE Select ENSP00000245907.4:n.774-162T=
ENST00000245907.10:c.774-162T= ENSP00000245907.4:n.774-162T=
ENST00000595577.1:n.278-162T=
ENST00000597442.5:n.23+95T=
NM_000064.3:c.774-162T= NP_000055.2:n.774-162T=
NM_000064.4:c.774-162T= MANE Select NP_000055.2:n.774-162T=
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