Canonical Allele Identifier: CA2663914813
Gene: PER2 HGNC NCBI

Linked Data

gnomAD v4: 2-238256842-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256847dup , CM000664.2:g.238256847dup GRCh38
NC_000002.11:g.239165488dup , CM000664.1:g.239165488dup GRCh37
NC_000002.10:g.238830227dup NCBI36
NG_012146.1:g.36724dup

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2065+79dup ENSP00000516757.1:n.2065+79dup
ENST00000707130.1:c.2065+79dup ENSP00000516758.1:n.2065+79dup
ENST00000254657.8:c.2065+79dup MANE Select ENSP00000254657.3:n.2065+79dup
ENST00000254657.7:c.2065+79dup ENSP00000254657.3:n.2065+79dup
NM_022817.2:c.2065+79dup NP_073728.1:n.2065+79dup
XM_005246111.3:c.2065+79dup XP_005246168.1:n.2065+79dup
XM_006712824.2:c.2065+79dup XP_006712887.1:n.2065+79dup
XM_005246111.4:c.2065+79dup XP_005246168.1:n.2065+79dup
XM_006712824.4:c.2065+79dup XP_006712887.1:n.2065+79dup
NM_022817.3:c.2065+79dup MANE Select NP_073728.1:n.2065+79dup
Search 100 bp 5'
Search 100 bp 3'