Canonical Allele Identifier: CA1338049478
Gene: PER2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238277972T= , CM000664.2:g.238277972T= GRCh38
NC_000002.11:g.239186613T= , CM000664.1:g.239186613T= GRCh37
NC_000002.10:g.238851352T= NCBI36
NG_012146.1:g.15595A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.-19-17A= ENSP00000516757.1:n.-19-17A=
ENST00000707130.1:c.-19-17A= ENSP00000516758.1:n.-19-17A=
ENST00000254657.8:c.-19-17A= MANE Select ENSP00000254657.3:n.-19-17A=
ENST00000254657.7:c.-19-17A= ENSP00000254657.3:n.-19-17A=
ENST00000431832.1:c.-19-17A= ENSP00000405891.1:n.-19-17A=
NM_022817.2:c.-19-17A= NP_073728.1:n.-19-17A=
XM_005246111.3:c.-19-17A= XP_005246168.1:n.-19-17A=
XM_006712824.2:c.-19-17A= XP_006712887.1:n.-19-17A=
XM_005246111.4:c.-19-17A= XP_005246168.1:n.-19-17A=
XM_006712824.4:c.-19-17A= XP_006712887.1:n.-19-17A=
NM_022817.3:c.-19-17A= MANE Select NP_073728.1:n.-19-17A=
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