Canonical Allele Identifier: CA351266433
Gene: PER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3211436
ClinVar RCV Id: RCV004505824
dbSNP Id: rs1362219255

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238277726G>A , CM000664.2:g.238277726G>A GRCh38
NC_000002.11:g.239186367G>A , CM000664.1:g.239186367G>A GRCh37
NC_000002.10:g.238851106G>A NCBI36
NG_012146.1:g.15841C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.211C>T ENSP00000516757.1:p.Pro71Ser
ENST00000707130.1:c.211C>T ENSP00000516758.1:p.Pro71Ser
ENST00000254657.8:c.211C>T MANE Select ENSP00000254657.3:p.Pro71Ser
ENST00000254657.7:c.211C>T ENSP00000254657.3:p.Pro71Ser
ENST00000355768.6:c.211C>T ENSP00000348013.2:p.Pro71Ser
ENST00000431832.1:c.211C>T ENSP00000405891.1:p.Pro71Ser
NM_022817.2:c.211C>T NP_073728.1:p.Pro71Ser
XM_005246111.3:c.211C>T XP_005246168.1:p.Pro71Ser
XM_006712824.2:c.211C>T XP_006712887.1:p.Pro71Ser
XM_005246111.4:c.211C>T XP_005246168.1:p.Pro71Ser
XM_006712824.4:c.211C>T XP_006712887.1:p.Pro71Ser
NM_022817.3:c.211C>T MANE Select NP_073728.1:p.Pro71Ser