Canonical Allele Identifier: CA2577294911
Gene: PER2 HGNC NCBI

Linked Data

gnomAD v4: 2-238256830-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256830C>T , CM000664.2:g.238256830C>T GRCh38
NC_000002.11:g.239165471C>T , CM000664.1:g.239165471C>T GRCh37
NC_000002.10:g.238830210C>T NCBI36
NG_012146.1:g.36737G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2065+92G>A ENSP00000516757.1:n.2065+92G>A
ENST00000707130.1:c.2065+92G>A ENSP00000516758.1:n.2065+92G>A
ENST00000254657.8:c.2065+92G>A MANE Select ENSP00000254657.3:n.2065+92G>A
ENST00000254657.7:c.2065+92G>A ENSP00000254657.3:n.2065+92G>A
NM_022817.2:c.2065+92G>A NP_073728.1:n.2065+92G>A
XM_005246111.3:c.2065+92G>A XP_005246168.1:n.2065+92G>A
XM_006712824.2:c.2065+92G>A XP_006712887.1:n.2065+92G>A
XM_005246111.4:c.2065+92G>A XP_005246168.1:n.2065+92G>A
XM_006712824.4:c.2065+92G>A XP_006712887.1:n.2065+92G>A
NM_022817.3:c.2065+92G>A MANE Select NP_073728.1:n.2065+92G>A
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