Canonical Allele Identifier: CA8739938
Gene: COG1 HGNC NCBI

Linked Data

dbSNP Id: rs756680020

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73196511A>G , CM000679.2:g.73196511A>G GRCh38
NC_000017.10:g.71192650A>G , CM000679.1:g.71192650A>G GRCh37
NC_000017.9:g.68704245A>G NCBI36
NG_008971.1:g.8478A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.320A>G MANE Select ENSP00000299886.4:p.Gln107Arg
ENST00000299886.8:c.320A>G ENSP00000299886.4:p.Gln107Arg
ENST00000438720.7:c.318A>G
ENST00000582587.2:c.317A>G
ENST00000618996.4:c.320A>G ENSP00000479450.1:p.Gln107Arg
NM_018714.2:c.320A>G NP_061184.1:p.Gln107Arg
NM_018714.3:c.320A>G MANE Select NP_061184.1:p.Gln107Arg