Canonical Allele Identifier: CA2663886992
Gene: PER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273115_238273116insTAC , CM000664.2:g.238273115_238273116insTAC GRCh38
NC_000002.11:g.239181756_239181757insTAC , CM000664.1:g.239181756_239181757insTAC GRCh37
NC_000002.10:g.238846495_238846496insTAC NCBI36
NG_012146.1:g.20452_20453insTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.525_526insTAG
ENST00000707130.1:c.525_526insTAG
ENST00000254657.8:c.525_526insTAG
ENST00000254657.7:c.525_526insTAG
ENST00000355768.6:c.525_526insTAG
NM_022817.2:c.525_526insTAG
XM_005246111.3:c.525_526insTAG
XM_006712824.2:c.525_526insTAG
XM_005246111.4:c.525_526insTAG
XM_006712824.4:c.525_526insTAG
NM_022817.3:c.525_526insTAG