Canonical Allele Identifier: CA2320568352
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713973C= , CM000681.2:g.6713973C= GRCh38
NC_000019.9:g.6713984C= , CM000681.1:g.6713984C= GRCh37
NC_000019.8:g.6664984C= NCBI36
NG_009557.1:g.11679G= , LRG_27:g.11679G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+19G= ENSP00000512083.1:n.650+19G=
ENST00000245907.11:c.773+19G= MANE Select ENSP00000245907.4:n.773+19G=
ENST00000245907.10:c.773+19G= ENSP00000245907.4:n.773+19G=
ENST00000595577.1:n.277+19G=
NM_000064.3:c.773+19G= NP_000055.2:n.773+19G=
NM_000064.4:c.773+19G= MANE Select NP_000055.2:n.773+19G=
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