Canonical Allele Identifier: CA431996440
Gene: PER2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.239184505T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238275864T>C , CM000664.2:g.238275864T>C GRCh38
NC_000002.11:g.239184505T>C , CM000664.1:g.239184505T>C GRCh37
NC_000002.10:g.238849244T>C NCBI36
NG_012146.1:g.17703A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.327A>G ENSP00000516757.1:p.Lys109=
ENST00000707130.1:c.327A>G ENSP00000516758.1:p.Lys109=
ENST00000254657.8:c.327A>G MANE Select ENSP00000254657.3:p.Lys109=
ENST00000254657.7:c.327A>G ENSP00000254657.3:p.Lys109=
ENST00000355768.6:c.327A>G ENSP00000348013.2:p.Lys109=
ENST00000431832.1:c.327A>G ENSP00000405891.1:p.Lys109=
NM_022817.2:c.327A>G NP_073728.1:p.Lys109=
XM_005246111.3:c.327A>G XP_005246168.1:p.Lys109=
XM_006712824.2:c.327A>G XP_006712887.1:p.Lys109=
XM_005246111.4:c.327A>G XP_005246168.1:p.Lys109=
XM_006712824.4:c.327A>G XP_006712887.1:p.Lys109=
NM_022817.3:c.327A>G MANE Select NP_073728.1:p.Lys109=