Canonical Allele Identifier: CA2197199
Gene: PER2 HGNC NCBI

Linked Data

dbSNP Id: rs139338215

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256929C>T , CM000664.2:g.238256929C>T GRCh38
NC_000002.11:g.239165570C>T , CM000664.1:g.239165570C>T GRCh37
NC_000002.10:g.238830309C>T NCBI36
NG_012146.1:g.36638G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2058G>A ENSP00000516757.1:p.Pro686=
ENST00000707130.1:c.2058G>A ENSP00000516758.1:p.Pro686=
ENST00000254657.8:c.2058G>A MANE Select ENSP00000254657.3:p.Pro686=
ENST00000254657.7:c.2058G>A ENSP00000254657.3:p.Pro686=
NM_022817.2:c.2058G>A NP_073728.1:p.Pro686=
XM_005246111.3:c.2058G>A XP_005246168.1:p.Pro686=
XM_006712824.2:c.2058G>A XP_006712887.1:p.Pro686=
XM_005246111.4:c.2058G>A XP_005246168.1:p.Pro686=
XM_006712824.4:c.2058G>A XP_006712887.1:p.Pro686=
NM_022817.3:c.2058G>A MANE Select NP_073728.1:p.Pro686=