Canonical Allele Identifier: CA1226660298
Gene: COG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230689981G= , CM000663.2:g.230689981G= GRCh38
NC_000001.10:g.230825727G= , CM000663.1:g.230825727G= GRCh37
NC_000001.9:g.228892350G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366669.9:c.1795-33G= MANE Select ENSP00000355629.4:n.1795-33G=
ENST00000366668.7:c.1792-33G= ENSP00000355628.3:n.1792-33G=
ENST00000366669.8:c.1795-33G= ENSP00000355629.4:n.1795-33G=
ENST00000468893.6:c.*1653-33G= ENSP00000476305.1:n.*1653-33G=
ENST00000478710.1:n.21G=
ENST00000490900.1:n.574-33G=
ENST00000534989.1:c.1618-33G= ENSP00000440349.1:n.1618-33G=
NM_001145036.1:c.1792-33G= NP_001138508.1:n.1792-33G=
NM_007357.2:c.1795-33G= NP_031383.1:n.1795-33G=
NM_007357.3:c.1795-33G= MANE Select NP_031383.1:n.1795-33G=
NM_001145036.2:c.1792-33G= NP_001138508.1:n.1792-33G=
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