Canonical Allele Identifier: CA345198970
Gene: COG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230690131A>T , CM000663.2:g.230690131A>T GRCh38
NC_000001.10:g.230825877A>T , CM000663.1:g.230825877A>T GRCh37
NC_000001.9:g.228892500A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366669.9:c.1912A>T MANE Select ENSP00000355629.4:p.Thr638Ser
ENST00000366668.7:c.1909A>T ENSP00000355628.3:p.Thr637Ser
ENST00000366669.8:c.1912A>T ENSP00000355629.4:p.Thr638Ser
ENST00000468893.6:c.*1770A>T ENSP00000476305.1:n.*1770A>T
ENST00000478710.1:n.171A>T
ENST00000490900.1:n.691A>T
ENST00000534989.1:c.1735A>T ENSP00000440349.1:p.Thr579Ser
NM_001145036.1:c.1909A>T NP_001138508.1:p.Thr637Ser
NM_007357.2:c.1912A>T NP_031383.1:p.Thr638Ser
NM_007357.3:c.1912A>T MANE Select NP_031383.1:p.Thr638Ser
NM_001145036.2:c.1909A>T NP_001138508.1:p.Thr637Ser