Canonical Allele Identifier: CA1338039071
Gene: PER2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256771C= , CM000664.2:g.238256771C= GRCh38
NC_000002.11:g.239165412C= , CM000664.1:g.239165412C= GRCh37
NC_000002.10:g.238830151C= NCBI36
NG_012146.1:g.36796G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.2065+151G= ENSP00000516757.1:n.2065+151G=
ENST00000707130.1:c.2065+151G= ENSP00000516758.1:n.2065+151G=
ENST00000254657.8:c.2065+151G= MANE Select ENSP00000254657.3:n.2065+151G=
ENST00000254657.7:c.2065+151G= ENSP00000254657.3:n.2065+151G=
NM_022817.2:c.2065+151G= NP_073728.1:n.2065+151G=
XM_005246111.3:c.2065+151G= XP_005246168.1:n.2065+151G=
XM_006712824.2:c.2065+151G= XP_006712887.1:n.2065+151G=
XM_005246111.4:c.2065+151G= XP_005246168.1:n.2065+151G=
XM_006712824.4:c.2065+151G= XP_006712887.1:n.2065+151G=
NM_022817.3:c.2065+151G= MANE Select NP_073728.1:n.2065+151G=
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