Canonical Allele Identifier: CA568575
Gene: PER3 HGNC NCBI

Linked Data

dbSNP Id: rs2640908
gnomAD v2: 1-7889941-C-T
gnomAD v3: 1-7829881-C-T
gnomAD v4: 1-7829881-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7829881C>T , CM000663.2:g.7829881C>T GRCh38
NC_000001.10:g.7889941C>T , CM000663.1:g.7889941C>T GRCh37
NC_000001.9:g.7812528C>T NCBI36
NG_046850.1:g.50502C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377532.8:c.2934C>T MANE Select ENSP00000366755.3:p.Thr978=
ENST00000361923.2:c.2907C>T ENSP00000355031.2:p.Thr969=
ENST00000377532.7:c.2934C>T ENSP00000366755.3:p.Thr978=
ENST00000613533.4:c.2934C>T ENSP00000482093.1:p.Thr978=
ENST00000614998.4:c.2931C>T ENSP00000479223.1:p.Thr977=
NM_001289861.1:c.2931C>T NP_001276790.1:p.Thr977=
NM_001289862.1:c.2934C>T NP_001276791.1:p.Thr978=
NM_001289863.1:c.2910C>T NP_001276792.1:p.Thr970=
NM_001289864.1:c.1974C>T NP_001276793.1:p.Thr658=
NM_016831.2:c.2907C>T NP_058515.1:p.Thr969=
XM_005263521.2:c.2931C>T XP_005263578.1:p.Thr977=
XM_005263522.2:c.2931C>T XP_005263579.1:p.Thr977=
XM_005263523.2:c.2913C>T XP_005263580.1:p.Thr971=
XM_005263524.2:c.2934C>T XP_005263581.1:p.Thr978=
XM_005263529.2:c.2409C>T XP_005263586.1:p.Thr803=
XM_011542384.1:c.2934C>T XP_011540686.1:p.Thr978=
XM_011542385.1:c.2931C>T XP_011540687.1:p.Thr977=
XM_011542386.1:c.2910C>T XP_011540688.1:p.Thr970=
XM_011542387.1:c.2766C>T XP_011540689.1:p.Thr922=
XM_011542388.1:c.2586C>T XP_011540690.1:p.Thr862=
XM_011542389.1:c.2571C>T XP_011540691.1:p.Thr857=
XM_011542390.1:c.2910C>T XP_011540692.1:p.Thr970=
XM_005263524.4:c.2934C>T XP_005263581.1:p.Thr978=
XM_017002723.2:c.2931C>T XP_016858212.1:p.Thr977=
XM_017002724.2:c.2928C>T XP_016858213.1:p.Thr976=
XM_017002726.2:c.2910C>T XP_016858215.1:p.Thr970=
XM_017002727.1:c.2766C>T XP_016858216.1:p.Thr922=
XM_017002728.1:c.2586C>T XP_016858217.1:p.Thr862=
XM_017002729.1:c.2571C>T XP_016858218.1:p.Thr857=
XM_017002730.2:c.2583C>T XP_016858219.1:p.Thr861=
XM_017002731.2:c.2562C>T XP_016858220.1:p.Thr854=
XM_017002732.1:c.2565C>T XP_016858221.1:p.Thr855=
XM_017002733.2:c.2409C>T XP_016858222.1:p.Thr803=
XM_017002734.1:c.2409C>T XP_016858223.1:p.Thr803=
XM_017002735.2:c.2406C>T XP_016858224.1:p.Thr802=
XM_017002737.1:c.1542C>T XP_016858226.1:p.Thr514=
XM_017002738.2:c.1539C>T XP_016858227.1:p.Thr513=
XM_024450585.1:c.2934C>T XP_024306353.1:p.Thr978=
XM_024450586.1:c.2931C>T XP_024306354.1:p.Thr977=
XM_024450587.1:c.2913C>T XP_024306355.1:p.Thr971=
XM_024450588.1:c.2910C>T XP_024306356.1:p.Thr970=
XM_024450590.1:c.2907C>T XP_024306358.1:p.Thr969=
XM_024450611.1:c.2388C>T XP_024306379.1:p.Thr796=
XM_024450612.1:c.2385C>T XP_024306380.1:p.Thr795=
NM_001289861.2:c.2931C>T NP_001276790.1:p.Thr977=
NM_001289862.2:c.2934C>T NP_001276791.1:p.Thr978=
NM_001289863.3:c.2910C>T NP_001276792.1:p.Thr970=
NM_001289864.3:c.1974C>T NP_001276793.1:p.Thr658=
NM_001377275.1:c.2934C>T MANE Select NP_001364204.1:p.Thr978=
NM_001377276.1:c.2910C>T NP_001364205.1:p.Thr970=
NM_016831.4:c.2907C>T NP_058515.1:p.Thr969=