Canonical Allele Identifier: CA431995150

Gene: PER2

Linked Data

• MyVariant Identifiers: chr2:g.239165566A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256925A>G , CM000664.2:g.238256925A>G	GRCh38
NC_000002.11:g.239165566A>G , CM000664.1:g.239165566A>G	GRCh37
NC_000002.10:g.238830305A>G	NCBI36
NG_012146.1:g.36642T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2062T>C	ENSP00000516757.1:p.Leu688=
ENST00000707130.1:c.2062T>C	ENSP00000516758.1:p.Leu688=
ENST00000254657.8:c.2062T>C MANE Select	ENSP00000254657.3:p.Leu688=
ENST00000254657.7:c.2062T>C	ENSP00000254657.3:p.Leu688=
NM_022817.2:c.2062T>C	NP_073728.1:p.Leu688=
XM_005246111.3:c.2062T>C	XP_005246168.1:p.Leu688=
XM_006712824.2:c.2062T>C	XP_006712887.1:p.Leu688=
XM_005246111.4:c.2062T>C	XP_005246168.1:p.Leu688=
XM_006712824.4:c.2062T>C	XP_006712887.1:p.Leu688=
NM_022817.3:c.2062T>C MANE Select	NP_073728.1:p.Leu688=