Canonical Allele Identifier: CA351266529
Gene: PER2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.239186384A>T (hg19) chr2:g.238277743A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238277743A>T , CM000664.2:g.238277743A>T GRCh38
NC_000002.11:g.239186384A>T , CM000664.1:g.239186384A>T GRCh37
NC_000002.10:g.238851123A>T NCBI36
NG_012146.1:g.15824T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.194T>A ENSP00000516757.1:p.Leu65Gln
ENST00000707130.1:c.194T>A ENSP00000516758.1:p.Leu65Gln
ENST00000254657.8:c.194T>A MANE Select ENSP00000254657.3:p.Leu65Gln
ENST00000254657.7:c.194T>A ENSP00000254657.3:p.Leu65Gln
ENST00000355768.6:c.194T>A ENSP00000348013.2:p.Leu65Gln
ENST00000431832.1:c.194T>A ENSP00000405891.1:p.Leu65Gln
NM_022817.2:c.194T>A NP_073728.1:p.Leu65Gln
XM_005246111.3:c.194T>A XP_005246168.1:p.Leu65Gln
XM_006712824.2:c.194T>A XP_006712887.1:p.Leu65Gln
XM_005246111.4:c.194T>A XP_005246168.1:p.Leu65Gln
XM_006712824.4:c.194T>A XP_006712887.1:p.Leu65Gln
NM_022817.3:c.194T>A MANE Select NP_073728.1:p.Leu65Gln
Search 100 bp 5'
Search 100 bp 3'