Canonical Allele Identifier: CA67990325

Gene: PER2

Linked Data

• dbSNP Id: rs778231252
• MyVariant Identifiers: chr2:g.238277668A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277668A>C , CM000664.2:g.238277668A>C	GRCh38
NC_000002.11:g.239186309A>C , CM000664.1:g.239186309A>C	GRCh37
NC_000002.10:g.238851048A>C	NCBI36
NG_012146.1:g.15899T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.230+39T>G	ENSP00000516757.1:n.230+39T>G
ENST00000707130.1:c.230+39T>G	ENSP00000516758.1:n.230+39T>G
ENST00000254657.8:c.230+39T>G MANE Select	ENSP00000254657.3:n.230+39T>G
ENST00000254657.7:c.230+39T>G	ENSP00000254657.3:n.230+39T>G
ENST00000355768.6:c.230+39T>G	ENSP00000348013.2:n.230+39T>G
ENST00000431832.1:c.230+39T>G	ENSP00000405891.1:n.230+39T>G
NM_022817.2:c.230+39T>G	NP_073728.1:n.230+39T>G
XM_005246111.3:c.230+39T>G	XP_005246168.1:n.230+39T>G
XM_006712824.2:c.230+39T>G	XP_006712887.1:n.230+39T>G
XM_005246111.4:c.230+39T>G	XP_005246168.1:n.230+39T>G
XM_006712824.4:c.230+39T>G	XP_006712887.1:n.230+39T>G
NM_022817.3:c.230+39T>G MANE Select	NP_073728.1:n.230+39T>G