Canonical Allele Identifier: CA224505781
Gene: UCP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2191040
ClinVar RCV Id: RCV002616705
dbSNP Id: rs369398270

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.73978072C>T , CM000673.2:g.73978072C>T GRCh38
NC_000011.9:g.73689117C>T , CM000673.1:g.73689117C>T GRCh37
NC_000011.8:g.73366765C>T NCBI36
NG_011478.1:g.9773G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310473.9:c.151G>A ENSP00000312029.3:p.Val51Met
ENST00000663595.2:c.151G>A MANE Select ENSP00000499695.1:p.Val51Met
ENST00000310473.7:c.151G>A ENSP00000312029.3:p.Val51Met
ENST00000536983.5:c.151G>A ENSP00000441147.1:p.Val51Met
ENST00000544615.5:c.70G>A ENSP00000439951.1:p.Val24Met
NM_003355.2:c.151G>A NP_003346.2:p.Val51Met
XM_024448674.1:c.154G>A XP_024304442.1:p.Val52Met
NM_001381943.1:c.151G>A NP_001368872.1:p.Val51Met
NM_001381944.1:c.151G>A NP_001368873.1:p.Val51Met
NM_001381945.1:c.151G>A NP_001368874.1:p.Val51Met
NM_001381947.1:c.151G>A NP_001368876.1:p.Val51Met
NM_001381948.1:c.151G>A NP_001368877.1:p.Val51Met
NM_001381949.1:c.151G>A NP_001368878.1:p.Val51Met
NM_001381950.1:c.151G>A NP_001368879.1:p.Val51Met
NM_003355.3:c.151G>A MANE Select NP_003346.2:p.Val51Met