Canonical Allele Identifier: CA1338039102

Gene: PER2

Linked Data

• dbSNP Id: rs1695775533
• gnomAD v4: 2-238256819-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256819A>G , CM000664.2:g.238256819A>G	GRCh38
NC_000002.11:g.239165460A>G , CM000664.1:g.239165460A>G	GRCh37
NC_000002.10:g.238830199A>G	NCBI36
NG_012146.1:g.36748T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2065+103T>C	ENSP00000516757.1:n.2065+103T>C
ENST00000707130.1:c.2065+103T>C	ENSP00000516758.1:n.2065+103T>C
ENST00000254657.8:c.2065+103T>C MANE Select	ENSP00000254657.3:n.2065+103T>C
ENST00000254657.7:c.2065+103T>C	ENSP00000254657.3:n.2065+103T>C
NM_022817.2:c.2065+103T>C	NP_073728.1:n.2065+103T>C
XM_005246111.3:c.2065+103T>C	XP_005246168.1:n.2065+103T>C
XM_006712824.2:c.2065+103T>C	XP_006712887.1:n.2065+103T>C
XM_005246111.4:c.2065+103T>C	XP_005246168.1:n.2065+103T>C
XM_006712824.4:c.2065+103T>C	XP_006712887.1:n.2065+103T>C
NM_022817.3:c.2065+103T>C MANE Select	NP_073728.1:n.2065+103T>C