Canonical Allele Identifier: CA766681714

Gene: PER2

Linked Data

• dbSNP Id: rs1265228005
• gnomAD v3: 2-238256834-T-G
• gnomAD v4: 2-238256834-T-G
• MyVariant Identifiers: chr2:g.239165475T>G (hg19) ; chr2:g.238256834T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256834T>G , CM000664.2:g.238256834T>G	GRCh38
NC_000002.11:g.239165475T>G , CM000664.1:g.239165475T>G	GRCh37
NC_000002.10:g.238830214T>G	NCBI36
NG_012146.1:g.36733A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2065+88A>C	ENSP00000516757.1:n.2065+88A>C
ENST00000707130.1:c.2065+88A>C	ENSP00000516758.1:n.2065+88A>C
ENST00000254657.8:c.2065+88A>C MANE Select	ENSP00000254657.3:n.2065+88A>C
ENST00000254657.7:c.2065+88A>C	ENSP00000254657.3:n.2065+88A>C
NM_022817.2:c.2065+88A>C	NP_073728.1:n.2065+88A>C
XM_005246111.3:c.2065+88A>C	XP_005246168.1:n.2065+88A>C
XM_006712824.2:c.2065+88A>C	XP_006712887.1:n.2065+88A>C
XM_005246111.4:c.2065+88A>C	XP_005246168.1:n.2065+88A>C
XM_006712824.4:c.2065+88A>C	XP_006712887.1:n.2065+88A>C
NM_022817.3:c.2065+88A>C MANE Select	NP_073728.1:n.2065+88A>C