Canonical Allele Identifier: CA431996453

Gene: PER2

Linked Data

• MyVariant Identifiers: chr2:g.239184529C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238275888C>T , CM000664.2:g.238275888C>T	GRCh38
NC_000002.11:g.239184529C>T , CM000664.1:g.239184529C>T	GRCh37
NC_000002.10:g.238849268C>T	NCBI36
NG_012146.1:g.17679G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.303G>A	ENSP00000516757.1:p.Gln101=
ENST00000707130.1:c.303G>A	ENSP00000516758.1:p.Gln101=
ENST00000254657.8:c.303G>A MANE Select	ENSP00000254657.3:p.Gln101=
ENST00000254657.7:c.303G>A	ENSP00000254657.3:p.Gln101=
ENST00000355768.6:c.303G>A	ENSP00000348013.2:p.Gln101=
ENST00000431832.1:c.303G>A	ENSP00000405891.1:p.Gln101=
NM_022817.2:c.303G>A	NP_073728.1:p.Gln101=
XM_005246111.3:c.303G>A	XP_005246168.1:p.Gln101=
XM_006712824.2:c.303G>A	XP_006712887.1:p.Gln101=
XM_005246111.4:c.303G>A	XP_005246168.1:p.Gln101=
XM_006712824.4:c.303G>A	XP_006712887.1:p.Gln101=
NM_022817.3:c.303G>A MANE Select	NP_073728.1:p.Gln101=