Canonical Allele Identifier: CA1338038973

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256673T= , CM000664.2:g.238256673T=	GRCh38
NC_000002.11:g.239165314T= , CM000664.1:g.239165314T=	GRCh37
NC_000002.10:g.238830053T=	NCBI36
NG_012146.1:g.36894A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.2065+249A=	ENSP00000516757.1:n.2065+249A=
ENST00000707130.1:c.2065+249A=	ENSP00000516758.1:n.2065+249A=
ENST00000254657.8:c.2065+249A= MANE Select	ENSP00000254657.3:n.2065+249A=
ENST00000254657.7:c.2065+249A=	ENSP00000254657.3:n.2065+249A=
NM_022817.2:c.2065+249A=	NP_073728.1:n.2065+249A=
XM_005246111.3:c.2065+249A=	XP_005246168.1:n.2065+249A=
XM_006712824.2:c.2065+249A=	XP_006712887.1:n.2065+249A=
XM_005246111.4:c.2065+249A=	XP_005246168.1:n.2065+249A=
XM_006712824.4:c.2065+249A=	XP_006712887.1:n.2065+249A=
NM_022817.3:c.2065+249A= MANE Select	NP_073728.1:n.2065+249A=