Canonical Allele Identifier: CA766699215

Gene: PER2

Linked Data

• dbSNP Id: rs1177143701
• gnomAD v4: 2-238275970-G-T
• MyVariant Identifiers: chr2:g.239184611G>T (hg19) ; chr2:g.238275970G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238275970G>T , CM000664.2:g.238275970G>T	GRCh38
NC_000002.11:g.239184611G>T , CM000664.1:g.239184611G>T	GRCh37
NC_000002.10:g.238849350G>T	NCBI36
NG_012146.1:g.17597C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.294-73C>A	ENSP00000516757.1:n.294-73C>A
ENST00000707130.1:c.294-73C>A	ENSP00000516758.1:n.294-73C>A
ENST00000254657.8:c.294-73C>A MANE Select	ENSP00000254657.3:n.294-73C>A
ENST00000254657.7:c.294-73C>A	ENSP00000254657.3:n.294-73C>A
ENST00000355768.6:c.294-73C>A	ENSP00000348013.2:n.294-73C>A
ENST00000431832.1:c.294-73C>A	ENSP00000405891.1:n.294-73C>A
NM_022817.2:c.294-73C>A	NP_073728.1:n.294-73C>A
XM_005246111.3:c.294-73C>A	XP_005246168.1:n.294-73C>A
XM_006712824.2:c.294-73C>A	XP_006712887.1:n.294-73C>A
XM_005246111.4:c.294-73C>A	XP_005246168.1:n.294-73C>A
XM_006712824.4:c.294-73C>A	XP_006712887.1:n.294-73C>A
NM_022817.3:c.294-73C>A MANE Select	NP_073728.1:n.294-73C>A