Canonical Allele Identifier: CA224505776

Gene: UCP2

Linked Data

• dbSNP Id: rs950320982
• gnomAD v2: 11-73689116-A-G
• gnomAD v3: 11-73978071-A-G
• gnomAD v4: 11-73978071-A-G
• MyVariant Identifiers: chr11:g.73689116A>G (hg19) ; chr11:g.73978071A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.73978071A>G , CM000673.2:g.73978071A>G	GRCh38
NC_000011.9:g.73689116A>G , CM000673.1:g.73689116A>G	GRCh37
NC_000011.8:g.73366764A>G	NCBI36
NG_011478.1:g.9774T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310473.9:c.152T>C	ENSP00000312029.3:p.Val51Ala
ENST00000663595.2:c.152T>C MANE Select	ENSP00000499695.1:p.Val51Ala
ENST00000310473.7:c.152T>C	ENSP00000312029.3:p.Val51Ala
ENST00000536983.5:c.152T>C	ENSP00000441147.1:p.Val51Ala
ENST00000544615.5:c.71T>C	ENSP00000439951.1:p.Val24Ala
NM_003355.2:c.152T>C	NP_003346.2:p.Val51Ala
XM_024448674.1:c.155T>C	XP_024304442.1:p.Val52Ala
NM_001381943.1:c.152T>C	NP_001368872.1:p.Val51Ala
NM_001381944.1:c.152T>C	NP_001368873.1:p.Val51Ala
NM_001381945.1:c.152T>C	NP_001368874.1:p.Val51Ala
NM_001381947.1:c.152T>C	NP_001368876.1:p.Val51Ala
NM_001381948.1:c.152T>C	NP_001368877.1:p.Val51Ala
NM_001381949.1:c.152T>C	NP_001368878.1:p.Val51Ala
NM_001381950.1:c.152T>C	NP_001368879.1:p.Val51Ala
NM_003355.3:c.152T>C MANE Select	NP_003346.2:p.Val51Ala