Canonical Allele Identifier: CA1338048519

Gene: PER2

Linked Data

• dbSNP Id: rs1696442565

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238275968T>C , CM000664.2:g.238275968T>C	GRCh38
NC_000002.11:g.239184609T>C , CM000664.1:g.239184609T>C	GRCh37
NC_000002.10:g.238849348T>C	NCBI36
NG_012146.1:g.17599A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.294-71A>G	ENSP00000516757.1:n.294-71A>G
ENST00000707130.1:c.294-71A>G	ENSP00000516758.1:n.294-71A>G
ENST00000254657.8:c.294-71A>G MANE Select	ENSP00000254657.3:n.294-71A>G
ENST00000254657.7:c.294-71A>G	ENSP00000254657.3:n.294-71A>G
ENST00000355768.6:c.294-71A>G	ENSP00000348013.2:n.294-71A>G
ENST00000431832.1:c.294-71A>G	ENSP00000405891.1:n.294-71A>G
NM_022817.2:c.294-71A>G	NP_073728.1:n.294-71A>G
XM_005246111.3:c.294-71A>G	XP_005246168.1:n.294-71A>G
XM_006712824.2:c.294-71A>G	XP_006712887.1:n.294-71A>G
XM_005246111.4:c.294-71A>G	XP_005246168.1:n.294-71A>G
XM_006712824.4:c.294-71A>G	XP_006712887.1:n.294-71A>G
NM_022817.3:c.294-71A>G MANE Select	NP_073728.1:n.294-71A>G