Canonical Allele Identifier: CA431996358

Gene: PER2

Linked Data

• MyVariant Identifiers: chr2:g.239181831G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273190G>C , CM000664.2:g.238273190G>C	GRCh38
NC_000002.11:g.239181831G>C , CM000664.1:g.239181831G>C	GRCh37
NC_000002.10:g.238846570G>C	NCBI36
NG_012146.1:g.20377C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.450C>G	ENSP00000516757.1:p.Ala150=
ENST00000707130.1:c.450C>G	ENSP00000516758.1:p.Ala150=
ENST00000254657.8:c.450C>G MANE Select	ENSP00000254657.3:p.Ala150=
ENST00000254657.7:c.450C>G	ENSP00000254657.3:p.Ala150=
ENST00000355768.6:c.450C>G	ENSP00000348013.2:p.Ala150=
NM_022817.2:c.450C>G	NP_073728.1:p.Ala150=
XM_005246111.3:c.450C>G	XP_005246168.1:p.Ala150=
XM_006712824.2:c.450C>G	XP_006712887.1:p.Ala150=
XM_005246111.4:c.450C>G	XP_005246168.1:p.Ala150=
XM_006712824.4:c.450C>G	XP_006712887.1:p.Ala150=
NM_022817.3:c.450C>G MANE Select	NP_073728.1:p.Ala150=