Canonical Allele Identifier: CA1338039115
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256828T= , CM000664.2:g.238256828T= GRCh38
NC_000002.11:g.239165469T= , CM000664.1:g.239165469T= GRCh37
NC_000002.10:g.238830208T= NCBI36
NG_012146.1:g.36739A=

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2065+94A= ENSP00000516757.1:n.2065+94A=
ENST00000707130.1:c.2065+94A= ENSP00000516758.1:n.2065+94A=
ENST00000254657.8:c.2065+94A= MANE Select ENSP00000254657.3:n.2065+94A=
ENST00000254657.7:c.2065+94A= ENSP00000254657.3:n.2065+94A=
NM_022817.2:c.2065+94A= NP_073728.1:n.2065+94A=
XM_005246111.3:c.2065+94A= XP_005246168.1:n.2065+94A=
XM_006712824.2:c.2065+94A= XP_006712887.1:n.2065+94A=
XM_005246111.4:c.2065+94A= XP_005246168.1:n.2065+94A=
XM_006712824.4:c.2065+94A= XP_006712887.1:n.2065+94A=
NM_022817.3:c.2065+94A= MANE Select NP_073728.1:n.2065+94A=