Canonical Allele Identifier: CA351267145

Gene: PER2

Linked Data

• MyVariant Identifiers: chr2:g.239186512C>G (hg19) ; chr2:g.238277871C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277871C>G , CM000664.2:g.238277871C>G	GRCh38
NC_000002.11:g.239186512C>G , CM000664.1:g.239186512C>G	GRCh37
NC_000002.10:g.238851251C>G	NCBI36
NG_012146.1:g.15696G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.66G>C	ENSP00000516757.1:p.Gln22His
ENST00000707130.1:c.66G>C	ENSP00000516758.1:p.Gln22His
ENST00000254657.8:c.66G>C MANE Select	ENSP00000254657.3:p.Gln22His
ENST00000254657.7:c.66G>C	ENSP00000254657.3:p.Gln22His
ENST00000355768.6:c.66G>C	ENSP00000348013.2:p.Gln22His
ENST00000431832.1:c.66G>C	ENSP00000405891.1:p.Gln22His
NM_022817.2:c.66G>C	NP_073728.1:p.Gln22His
XM_005246111.3:c.66G>C	XP_005246168.1:p.Gln22His
XM_006712824.2:c.66G>C	XP_006712887.1:p.Gln22His
XM_005246111.4:c.66G>C	XP_005246168.1:p.Gln22His
XM_006712824.4:c.66G>C	XP_006712887.1:p.Gln22His
NM_022817.3:c.66G>C MANE Select	NP_073728.1:p.Gln22His