Canonical Allele Identifier: CA766681777

Gene: PER2

Linked Data

• dbSNP Id: rs1267048026
• gnomAD v3: 2-238256915-G-A
• gnomAD v4: 2-238256915-G-A
• MyVariant Identifiers: chr2:g.239165556G>A (hg19) ; chr2:g.238256915G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256915G>A , CM000664.2:g.238256915G>A	GRCh38
NC_000002.11:g.239165556G>A , CM000664.1:g.239165556G>A	GRCh37
NC_000002.10:g.238830295G>A	NCBI36
NG_012146.1:g.36652C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2065+7C>T	ENSP00000516757.1:n.2065+7C>T
ENST00000707130.1:c.2065+7C>T	ENSP00000516758.1:n.2065+7C>T
ENST00000254657.8:c.2065+7C>T MANE Select	ENSP00000254657.3:n.2065+7C>T
ENST00000254657.7:c.2065+7C>T	ENSP00000254657.3:n.2065+7C>T
NM_022817.2:c.2065+7C>T	NP_073728.1:n.2065+7C>T
XM_005246111.3:c.2065+7C>T	XP_005246168.1:n.2065+7C>T
XM_006712824.2:c.2065+7C>T	XP_006712887.1:n.2065+7C>T
XM_005246111.4:c.2065+7C>T	XP_005246168.1:n.2065+7C>T
XM_006712824.4:c.2065+7C>T	XP_006712887.1:n.2065+7C>T
NM_022817.3:c.2065+7C>T MANE Select	NP_073728.1:n.2065+7C>T