Canonical Allele Identifier: CA2663888800

Gene: PER2

Linked Data

• gnomAD v4: 2-238278041-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238278041C>A , CM000664.2:g.238278041C>A	GRCh38
NC_000002.11:g.239186682C>A , CM000664.1:g.239186682C>A	GRCh37
NC_000002.10:g.238851421C>A	NCBI36
NG_012146.1:g.15526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.-19-86G>T	ENSP00000516757.1:n.-19-86G>T
ENST00000707130.1:c.-19-86G>T	ENSP00000516758.1:n.-19-86G>T
ENST00000254657.8:c.-19-86G>T MANE Select	ENSP00000254657.3:n.-19-86G>T
ENST00000254657.7:c.-19-86G>T	ENSP00000254657.3:n.-19-86G>T
ENST00000431832.1:c.-19-86G>T	ENSP00000405891.1:n.-19-86G>T
NM_022817.2:c.-19-86G>T	NP_073728.1:n.-19-86G>T
XM_005246111.3:c.-19-86G>T	XP_005246168.1:n.-19-86G>T
XM_006712824.2:c.-19-86G>T	XP_006712887.1:n.-19-86G>T
XM_005246111.4:c.-19-86G>T	XP_005246168.1:n.-19-86G>T
XM_006712824.4:c.-19-86G>T	XP_006712887.1:n.-19-86G>T
NM_022817.3:c.-19-86G>T MANE Select	NP_073728.1:n.-19-86G>T