Canonical Allele Identifier: CA351266718

Gene: PER2

Linked Data

• gnomAD v4: 2-238277786-G-C
• MyVariant Identifiers: chr2:g.239186427G>C (hg19) ; chr2:g.238277786G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277786G>C , CM000664.2:g.238277786G>C	GRCh38
NC_000002.11:g.239186427G>C , CM000664.1:g.239186427G>C	GRCh37
NC_000002.10:g.238851166G>C	NCBI36
NG_012146.1:g.15781C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.151C>G	ENSP00000516757.1:p.Arg51Gly
ENST00000707130.1:c.151C>G	ENSP00000516758.1:p.Arg51Gly
ENST00000254657.8:c.151C>G MANE Select	ENSP00000254657.3:p.Arg51Gly
ENST00000254657.7:c.151C>G	ENSP00000254657.3:p.Arg51Gly
ENST00000355768.6:c.151C>G	ENSP00000348013.2:p.Arg51Gly
ENST00000431832.1:c.151C>G	ENSP00000405891.1:p.Arg51Gly
NM_022817.2:c.151C>G	NP_073728.1:p.Arg51Gly
XM_005246111.3:c.151C>G	XP_005246168.1:p.Arg51Gly
XM_006712824.2:c.151C>G	XP_006712887.1:p.Arg51Gly
XM_005246111.4:c.151C>G	XP_005246168.1:p.Arg51Gly
XM_006712824.4:c.151C>G	XP_006712887.1:p.Arg51Gly
NM_022817.3:c.151C>G MANE Select	NP_073728.1:p.Arg51Gly