Canonical Allele Identifier: CA2197197
Gene: PER2 HGNC NCBI

Linked Data

dbSNP Id: rs770245419

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256908G>T , CM000664.2:g.238256908G>T GRCh38
NC_000002.11:g.239165549G>T , CM000664.1:g.239165549G>T GRCh37
NC_000002.10:g.238830288G>T NCBI36
NG_012146.1:g.36659C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2065+14C>A ENSP00000516757.1:n.2065+14C>A
ENST00000707130.1:c.2065+14C>A ENSP00000516758.1:n.2065+14C>A
ENST00000254657.8:c.2065+14C>A MANE Select ENSP00000254657.3:n.2065+14C>A
ENST00000254657.7:c.2065+14C>A ENSP00000254657.3:n.2065+14C>A
NM_022817.2:c.2065+14C>A NP_073728.1:n.2065+14C>A
XM_005246111.3:c.2065+14C>A XP_005246168.1:n.2065+14C>A
XM_006712824.2:c.2065+14C>A XP_006712887.1:n.2065+14C>A
XM_005246111.4:c.2065+14C>A XP_005246168.1:n.2065+14C>A
XM_006712824.4:c.2065+14C>A XP_006712887.1:n.2065+14C>A
NM_022817.3:c.2065+14C>A MANE Select NP_073728.1:n.2065+14C>A