Canonical Allele Identifier: CA2197742
Gene: PER2 HGNC NCBI

Linked Data

dbSNP Id: rs371163217

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273075T>C , CM000664.2:g.238273075T>C GRCh38
NC_000002.11:g.239181716T>C , CM000664.1:g.239181716T>C GRCh37
NC_000002.10:g.238846455T>C NCBI36
NG_012146.1:g.20492A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.565A>G ENSP00000516757.1:p.Asn189Asp
ENST00000707130.1:c.565A>G ENSP00000516758.1:p.Asn189Asp
ENST00000254657.8:c.565A>G MANE Select ENSP00000254657.3:p.Asn189Asp
ENST00000254657.7:c.565A>G ENSP00000254657.3:p.Asn189Asp
ENST00000355768.6:c.565A>G ENSP00000348013.2:p.Asn189Asp
NM_022817.2:c.565A>G NP_073728.1:p.Asn189Asp
XM_005246111.3:c.565A>G XP_005246168.1:p.Asn189Asp
XM_006712824.2:c.565A>G XP_006712887.1:p.Asn189Asp
XM_005246111.4:c.565A>G XP_005246168.1:p.Asn189Asp
XM_006712824.4:c.565A>G XP_006712887.1:p.Asn189Asp
NM_022817.3:c.565A>G MANE Select NP_073728.1:p.Asn189Asp