Canonical Allele Identifier: CA1043881433

Gene: PER2

Linked Data

• dbSNP Id: rs1020967073
• gnomAD v3: 2-238273513-G-A
• gnomAD v4: 2-238273513-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273513G>A , CM000664.2:g.238273513G>A	GRCh38
NC_000002.11:g.239182154G>A , CM000664.1:g.239182154G>A	GRCh37
NC_000002.10:g.238846893G>A	NCBI36
NG_012146.1:g.20054C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-322C>T	ENSP00000516757.1:n.449-322C>T
ENST00000707130.1:c.449-322C>T	ENSP00000516758.1:n.449-322C>T
ENST00000254657.8:c.449-322C>T MANE Select	ENSP00000254657.3:n.449-322C>T
ENST00000254657.7:c.449-322C>T	ENSP00000254657.3:n.449-322C>T
ENST00000355768.6:c.449-322C>T	ENSP00000348013.2:n.449-322C>T
NM_022817.2:c.449-322C>T	NP_073728.1:n.449-322C>T
XM_005246111.3:c.449-322C>T	XP_005246168.1:n.449-322C>T
XM_006712824.2:c.449-322C>T	XP_006712887.1:n.449-322C>T
XM_005246111.4:c.449-322C>T	XP_005246168.1:n.449-322C>T
XM_006712824.4:c.449-322C>T	XP_006712887.1:n.449-322C>T
NM_022817.3:c.449-322C>T MANE Select	NP_073728.1:n.449-322C>T