Canonical Allele Identifier: CA345198959
Gene: COG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230690126A>G , CM000663.2:g.230690126A>G GRCh38
NC_000001.10:g.230825872A>G , CM000663.1:g.230825872A>G GRCh37
NC_000001.9:g.228892495A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366669.9:c.1907A>G MANE Select ENSP00000355629.4:p.Glu636Gly
ENST00000366668.7:c.1904A>G ENSP00000355628.3:p.Glu635Gly
ENST00000366669.8:c.1907A>G ENSP00000355629.4:p.Glu636Gly
ENST00000468893.6:c.*1765A>G ENSP00000476305.1:n.*1765A>G
ENST00000478710.1:n.166A>G
ENST00000490900.1:n.686A>G
ENST00000534989.1:c.1730A>G ENSP00000440349.1:p.Glu577Gly
NM_001145036.1:c.1904A>G NP_001138508.1:p.Glu635Gly
NM_007357.2:c.1907A>G NP_031383.1:p.Glu636Gly
NM_007357.3:c.1907A>G MANE Select NP_031383.1:p.Glu636Gly
NM_001145036.2:c.1904A>G NP_001138508.1:p.Glu635Gly