Canonical Allele Identifier: CA431995247

Gene: PER2

Linked Data

• MyVariant Identifiers: chr2:g.239165723T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238257082T>C , CM000664.2:g.238257082T>C	GRCh38
NC_000002.11:g.239165723T>C , CM000664.1:g.239165723T>C	GRCh37
NC_000002.10:g.238830462T>C	NCBI36
NG_012146.1:g.36485A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.1905A>G	ENSP00000516757.1:p.Ala635=
ENST00000707130.1:c.1905A>G	ENSP00000516758.1:p.Ala635=
ENST00000254657.8:c.1905A>G MANE Select	ENSP00000254657.3:p.Ala635=
ENST00000254657.7:c.1905A>G	ENSP00000254657.3:p.Ala635=
NM_022817.2:c.1905A>G	NP_073728.1:p.Ala635=
XM_005246111.3:c.1905A>G	XP_005246168.1:p.Ala635=
XM_006712824.2:c.1905A>G	XP_006712887.1:p.Ala635=
XM_005246111.4:c.1905A>G	XP_005246168.1:p.Ala635=
XM_006712824.4:c.1905A>G	XP_006712887.1:p.Ala635=
NM_022817.3:c.1905A>G MANE Select	NP_073728.1:p.Ala635=