Canonical Allele Identifier: CA351264288

Gene: PER2

Linked Data

• MyVariant Identifiers: chr2:g.239181778G>C (hg19) ; chr2:g.238273137G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273137G>C , CM000664.2:g.238273137G>C	GRCh38
NC_000002.11:g.239181778G>C , CM000664.1:g.239181778G>C	GRCh37
NC_000002.10:g.238846517G>C	NCBI36
NG_012146.1:g.20430C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.503C>G	ENSP00000516757.1:p.Ala168Gly
ENST00000707130.1:c.503C>G	ENSP00000516758.1:p.Ala168Gly
ENST00000254657.8:c.503C>G MANE Select	ENSP00000254657.3:p.Ala168Gly
ENST00000254657.7:c.503C>G	ENSP00000254657.3:p.Ala168Gly
ENST00000355768.6:c.503C>G	ENSP00000348013.2:p.Ala168Gly
NM_022817.2:c.503C>G	NP_073728.1:p.Ala168Gly
XM_005246111.3:c.503C>G	XP_005246168.1:p.Ala168Gly
XM_006712824.2:c.503C>G	XP_006712887.1:p.Ala168Gly
XM_005246111.4:c.503C>G	XP_005246168.1:p.Ala168Gly
XM_006712824.4:c.503C>G	XP_006712887.1:p.Ala168Gly
NM_022817.3:c.503C>G MANE Select	NP_073728.1:p.Ala168Gly