Canonical Allele Identifier: CA2320568072
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713678C= , CM000681.2:g.6713678C= GRCh38
NC_000019.9:g.6713689C= , CM000681.1:g.6713689C= GRCh37
NC_000019.8:g.6664689C= NCBI36
NG_009557.1:g.11974G= , LRG_27:g.11974G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-169G= ENSP00000512083.1:n.651-169G=
ENST00000245907.11:c.774-169G= MANE Select ENSP00000245907.4:n.774-169G=
ENST00000245907.10:c.774-169G= ENSP00000245907.4:n.774-169G=
ENST00000595577.1:n.278-169G=
ENST00000597442.5:n.23+88G=
NM_000064.3:c.774-169G= NP_000055.2:n.774-169G=
NM_000064.4:c.774-169G= MANE Select NP_000055.2:n.774-169G=
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