Canonical Allele Identifier: CA8739904
Gene: COG1 HGNC NCBI

Linked Data

dbSNP Id: rs774109257

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193279C>G , CM000679.2:g.73193279C>G GRCh38
NC_000017.10:g.71189418C>G , CM000679.1:g.71189418C>G GRCh37
NC_000017.9:g.68701013C>G NCBI36
NG_008971.1:g.5246C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.210C>G MANE Select ENSP00000299886.4:p.Arg70=
ENST00000299886.8:c.210C>G ENSP00000299886.4:p.Arg70=
ENST00000438720.7:c.208C>G
ENST00000582587.2:c.187C>G
ENST00000618996.4:c.210C>G ENSP00000479450.1:p.Arg70=
NM_018714.2:c.210C>G NP_061184.1:p.Arg70=
NM_018714.3:c.210C>G MANE Select NP_061184.1:p.Arg70=