Canonical Allele Identifier: CA67990693

Gene: PER2

Linked Data

• dbSNP Id: rs570615419
• gnomAD v2: 2-239186593-G-A
• gnomAD v4: 2-238277952-G-A
• MyVariant Identifiers: chr2:g.239186593G>A (hg19) ; chr2:g.238277952G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277952G>A , CM000664.2:g.238277952G>A	GRCh38
NC_000002.11:g.239186593G>A , CM000664.1:g.239186593G>A	GRCh37
NC_000002.10:g.238851332G>A	NCBI36
NG_012146.1:g.15615C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.-16C>T	ENSP00000516757.1:n.-16C>T
ENST00000707130.1:c.-16C>T	ENSP00000516758.1:n.-16C>T
ENST00000254657.8:c.-16C>T MANE Select	ENSP00000254657.3:n.-16C>T
ENST00000254657.7:c.-16C>T	ENSP00000254657.3:n.-16C>T
ENST00000431832.1:c.-16C>T	ENSP00000405891.1:n.-16C>T
NM_022817.2:c.-16C>T	NP_073728.1:n.-16C>T
XM_005246111.3:c.-16C>T	XP_005246168.1:n.-16C>T
XM_006712824.2:c.-16C>T	XP_006712887.1:n.-16C>T
XM_005246111.4:c.-16C>T	XP_005246168.1:n.-16C>T
XM_006712824.4:c.-16C>T	XP_006712887.1:n.-16C>T
NM_022817.3:c.-16C>T MANE Select	NP_073728.1:n.-16C>T