Canonical Allele Identifier: CA351254152
Gene: PER2 HGNC NCBI

Linked Data

dbSNP Id: rs1695778986

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256927T>C , CM000664.2:g.238256927T>C GRCh38
NC_000002.11:g.239165568T>C , CM000664.1:g.239165568T>C GRCh37
NC_000002.10:g.238830307T>C NCBI36
NG_012146.1:g.36640A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2060A>G ENSP00000516757.1:p.Glu687Gly
ENST00000707130.1:c.2060A>G ENSP00000516758.1:p.Glu687Gly
ENST00000254657.8:c.2060A>G MANE Select ENSP00000254657.3:p.Glu687Gly
ENST00000254657.7:c.2060A>G ENSP00000254657.3:p.Glu687Gly
NM_022817.2:c.2060A>G NP_073728.1:p.Glu687Gly
XM_005246111.3:c.2060A>G XP_005246168.1:p.Glu687Gly
XM_006712824.2:c.2060A>G XP_006712887.1:p.Glu687Gly
XM_005246111.4:c.2060A>G XP_005246168.1:p.Glu687Gly
XM_006712824.4:c.2060A>G XP_006712887.1:p.Glu687Gly
NM_022817.3:c.2060A>G MANE Select NP_073728.1:p.Glu687Gly