Canonical Allele Identifier: CA431995154
Gene: PER2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.239165573C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256932C>T , CM000664.2:g.238256932C>T GRCh38
NC_000002.11:g.239165573C>T , CM000664.1:g.239165573C>T GRCh37
NC_000002.10:g.238830312C>T NCBI36
NG_012146.1:g.36635G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2055G>A ENSP00000516757.1:p.Gln685=
ENST00000707130.1:c.2055G>A ENSP00000516758.1:p.Gln685=
ENST00000254657.8:c.2055G>A MANE Select ENSP00000254657.3:p.Gln685=
ENST00000254657.7:c.2055G>A ENSP00000254657.3:p.Gln685=
NM_022817.2:c.2055G>A NP_073728.1:p.Gln685=
XM_005246111.3:c.2055G>A XP_005246168.1:p.Gln685=
XM_006712824.2:c.2055G>A XP_006712887.1:p.Gln685=
XM_005246111.4:c.2055G>A XP_005246168.1:p.Gln685=
XM_006712824.4:c.2055G>A XP_006712887.1:p.Gln685=
NM_022817.3:c.2055G>A MANE Select NP_073728.1:p.Gln685=