Canonical Allele Identifier: CA2320567881
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713352G= , CM000681.2:g.6713352G= GRCh38
NC_000019.9:g.6713363G= , CM000681.1:g.6713363G= GRCh37
NC_000019.8:g.6664363G= NCBI36
NG_009557.1:g.12300C= , LRG_27:g.12300C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.754-37C= ENSP00000512083.1:n.754-37C=
ENST00000695692.1:n.201-37C=
ENST00000245907.11:c.877-37C= MANE Select ENSP00000245907.4:n.877-37C=
ENST00000245907.10:c.877-37C= ENSP00000245907.4:n.877-37C=
ENST00000595577.1:n.381-37C=
ENST00000597442.5:n.127-37C=
NM_000064.3:c.877-37C= NP_000055.2:n.877-37C=
NM_000064.4:c.877-37C= MANE Select NP_000055.2:n.877-37C=
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