Canonical Allele Identifier: CA766697738

Gene: PER2

Linked Data

• dbSNP Id: rs1292895056
• gnomAD v3: 2-238273207-T-G
• gnomAD v4: 2-238273207-T-G
• MyVariant Identifiers: chr2:g.239181848T>G (hg19) ; chr2:g.238273207T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273207T>G , CM000664.2:g.238273207T>G	GRCh38
NC_000002.11:g.239181848T>G , CM000664.1:g.239181848T>G	GRCh37
NC_000002.10:g.238846587T>G	NCBI36
NG_012146.1:g.20360A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-16A>C	ENSP00000516757.1:n.449-16A>C
ENST00000707130.1:c.449-16A>C	ENSP00000516758.1:n.449-16A>C
ENST00000254657.8:c.449-16A>C MANE Select	ENSP00000254657.3:n.449-16A>C
ENST00000254657.7:c.449-16A>C	ENSP00000254657.3:n.449-16A>C
ENST00000355768.6:c.449-16A>C	ENSP00000348013.2:n.449-16A>C
NM_022817.2:c.449-16A>C	NP_073728.1:n.449-16A>C
XM_005246111.3:c.449-16A>C	XP_005246168.1:n.449-16A>C
XM_006712824.2:c.449-16A>C	XP_006712887.1:n.449-16A>C
XM_005246111.4:c.449-16A>C	XP_005246168.1:n.449-16A>C
XM_006712824.4:c.449-16A>C	XP_006712887.1:n.449-16A>C
NM_022817.3:c.449-16A>C MANE Select	NP_073728.1:n.449-16A>C