Canonical Allele Identifier: CA431995152

Gene: PER2

Linked Data

• dbSNP Id: rs139338215
• gnomAD v2: 2-239165570-C-G
• gnomAD v4: 2-238256929-C-G
• MyVariant Identifiers: chr2:g.239165570C>G (hg19) ; chr2:g.238256929C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256929C>G , CM000664.2:g.238256929C>G	GRCh38
NC_000002.11:g.239165570C>G , CM000664.1:g.239165570C>G	GRCh37
NC_000002.10:g.238830309C>G	NCBI36
NG_012146.1:g.36638G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2058G>C	ENSP00000516757.1:p.Pro686=
ENST00000707130.1:c.2058G>C	ENSP00000516758.1:p.Pro686=
ENST00000254657.8:c.2058G>C MANE Select	ENSP00000254657.3:p.Pro686=
ENST00000254657.7:c.2058G>C	ENSP00000254657.3:p.Pro686=
NM_022817.2:c.2058G>C	NP_073728.1:p.Pro686=
XM_005246111.3:c.2058G>C	XP_005246168.1:p.Pro686=
XM_006712824.2:c.2058G>C	XP_006712887.1:p.Pro686=
XM_005246111.4:c.2058G>C	XP_005246168.1:p.Pro686=
XM_006712824.4:c.2058G>C	XP_006712887.1:p.Pro686=
NM_022817.3:c.2058G>C MANE Select	NP_073728.1:p.Pro686=