Canonical Allele Identifier: CA67985510
Gene: PER2 HGNC NCBI

Linked Data

dbSNP Id: rs373357215

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273092G>C , CM000664.2:g.238273092G>C GRCh38
NC_000002.11:g.239181733G>C , CM000664.1:g.239181733G>C GRCh37
NC_000002.10:g.238846472G>C NCBI36
NG_012146.1:g.20475C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.548C>G ENSP00000516757.1:p.Ser183Cys
ENST00000707130.1:c.548C>G ENSP00000516758.1:p.Ser183Cys
ENST00000254657.8:c.548C>G MANE Select ENSP00000254657.3:p.Ser183Cys
ENST00000254657.7:c.548C>G ENSP00000254657.3:p.Ser183Cys
ENST00000355768.6:c.548C>G ENSP00000348013.2:p.Ser183Cys
NM_022817.2:c.548C>G NP_073728.1:p.Ser183Cys
XM_005246111.3:c.548C>G XP_005246168.1:p.Ser183Cys
XM_006712824.2:c.548C>G XP_006712887.1:p.Ser183Cys
XM_005246111.4:c.548C>G XP_005246168.1:p.Ser183Cys
XM_006712824.4:c.548C>G XP_006712887.1:p.Ser183Cys
NM_022817.3:c.548C>G MANE Select NP_073728.1:p.Ser183Cys