Canonical Allele Identifier: CA431995156

Gene: PER2

Linked Data

• gnomAD v4: 2-238256935-C-A
• MyVariant Identifiers: chr2:g.239165576C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256935C>A , CM000664.2:g.238256935C>A	GRCh38
NC_000002.11:g.239165576C>A , CM000664.1:g.239165576C>A	GRCh37
NC_000002.10:g.238830315C>A	NCBI36
NG_012146.1:g.36632G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2052G>T	ENSP00000516757.1:p.Pro684=
ENST00000707130.1:c.2052G>T	ENSP00000516758.1:p.Pro684=
ENST00000254657.8:c.2052G>T MANE Select	ENSP00000254657.3:p.Pro684=
ENST00000254657.7:c.2052G>T	ENSP00000254657.3:p.Pro684=
NM_022817.2:c.2052G>T	NP_073728.1:p.Pro684=
XM_005246111.3:c.2052G>T	XP_005246168.1:p.Pro684=
XM_006712824.2:c.2052G>T	XP_006712887.1:p.Pro684=
XM_005246111.4:c.2052G>T	XP_005246168.1:p.Pro684=
XM_006712824.4:c.2052G>T	XP_006712887.1:p.Pro684=
NM_022817.3:c.2052G>T MANE Select	NP_073728.1:p.Pro684=