Canonical Allele Identifier: CA67968772

Gene: PER2

Linked Data

• dbSNP Id: rs991280901
• gnomAD v3: 2-238256766-C-G
• gnomAD v4: 2-238256766-C-G
• MyVariant Identifiers: chr2:g.239165407C>G (hg19) ; chr2:g.238256766C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256766C>G , CM000664.2:g.238256766C>G	GRCh38
NC_000002.11:g.239165407C>G , CM000664.1:g.239165407C>G	GRCh37
NC_000002.10:g.238830146C>G	NCBI36
NG_012146.1:g.36801G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.2065+156G>C	ENSP00000516757.1:n.2065+156G>C
ENST00000707130.1:c.2065+156G>C	ENSP00000516758.1:n.2065+156G>C
ENST00000254657.8:c.2065+156G>C MANE Select	ENSP00000254657.3:n.2065+156G>C
ENST00000254657.7:c.2065+156G>C	ENSP00000254657.3:n.2065+156G>C
NM_022817.2:c.2065+156G>C	NP_073728.1:n.2065+156G>C
XM_005246111.3:c.2065+156G>C	XP_005246168.1:n.2065+156G>C
XM_006712824.2:c.2065+156G>C	XP_006712887.1:n.2065+156G>C
XM_005246111.4:c.2065+156G>C	XP_005246168.1:n.2065+156G>C
XM_006712824.4:c.2065+156G>C	XP_006712887.1:n.2065+156G>C
NM_022817.3:c.2065+156G>C MANE Select	NP_073728.1:n.2065+156G>C