Canonical Allele Identifier: CA351264463
Gene: PER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273172C>A , CM000664.2:g.238273172C>A GRCh38
NC_000002.11:g.239181813C>A , CM000664.1:g.239181813C>A GRCh37
NC_000002.10:g.238846552C>A NCBI36
NG_012146.1:g.20395G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.468G>T ENSP00000516757.1:p.Gln156His
ENST00000707130.1:c.468G>T ENSP00000516758.1:p.Gln156His
ENST00000254657.8:c.468G>T MANE Select ENSP00000254657.3:p.Gln156His
ENST00000254657.7:c.468G>T ENSP00000254657.3:p.Gln156His
ENST00000355768.6:c.468G>T ENSP00000348013.2:p.Gln156His
NM_022817.2:c.468G>T NP_073728.1:p.Gln156His
XM_005246111.3:c.468G>T XP_005246168.1:p.Gln156His
XM_006712824.2:c.468G>T XP_006712887.1:p.Gln156His
XM_005246111.4:c.468G>T XP_005246168.1:p.Gln156His
XM_006712824.4:c.468G>T XP_006712887.1:p.Gln156His
NM_022817.3:c.468G>T MANE Select NP_073728.1:p.Gln156His