Canonical Allele Identifier: CA351254303
Gene: PER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256994A>T , CM000664.2:g.238256994A>T GRCh38
NC_000002.11:g.239165635A>T , CM000664.1:g.239165635A>T GRCh37
NC_000002.10:g.238830374A>T NCBI36
NG_012146.1:g.36573T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.1993T>A ENSP00000516757.1:p.Ser665Thr
ENST00000707130.1:c.1993T>A ENSP00000516758.1:p.Ser665Thr
ENST00000254657.8:c.1993T>A MANE Select ENSP00000254657.3:p.Ser665Thr
ENST00000254657.7:c.1993T>A ENSP00000254657.3:p.Ser665Thr
NM_022817.2:c.1993T>A NP_073728.1:p.Ser665Thr
XM_005246111.3:c.1993T>A XP_005246168.1:p.Ser665Thr
XM_006712824.2:c.1993T>A XP_006712887.1:p.Ser665Thr
XM_005246111.4:c.1993T>A XP_005246168.1:p.Ser665Thr
XM_006712824.4:c.1993T>A XP_006712887.1:p.Ser665Thr
NM_022817.3:c.1993T>A MANE Select NP_073728.1:p.Ser665Thr