Canonical Allele Identifier: CA351254342
Gene: PER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238257012T>A , CM000664.2:g.238257012T>A GRCh38
NC_000002.11:g.239165653T>A , CM000664.1:g.239165653T>A GRCh37
NC_000002.10:g.238830392T>A NCBI36
NG_012146.1:g.36555A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.1975A>T ENSP00000516757.1:p.Lys659Ter
ENST00000707130.1:c.1975A>T ENSP00000516758.1:p.Lys659Ter
ENST00000254657.8:c.1975A>T MANE Select ENSP00000254657.3:p.Lys659Ter
ENST00000254657.7:c.1975A>T ENSP00000254657.3:p.Lys659Ter
NM_022817.2:c.1975A>T NP_073728.1:p.Lys659Ter
XM_005246111.3:c.1975A>T XP_005246168.1:p.Lys659Ter
XM_006712824.2:c.1975A>T XP_006712887.1:p.Lys659Ter
XM_005246111.4:c.1975A>T XP_005246168.1:p.Lys659Ter
XM_006712824.4:c.1975A>T XP_006712887.1:p.Lys659Ter
NM_022817.3:c.1975A>T MANE Select NP_073728.1:p.Lys659Ter