Canonical Allele Identifier: CA381814308
Gene: UCP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.73716797T>G (hg19) chr11:g.74005752T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74005752T>G , CM000673.2:g.74005752T>G GRCh38
NC_000011.9:g.73716797T>G , CM000673.1:g.73716797T>G GRCh37
NC_000011.8:g.73394445T>G NCBI36
NG_011515.1:g.8486A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000314032.9:c.519A>C MANE Select ENSP00000323740.4:p.Glu173Asp
ENST00000314032.8:c.519A>C ENSP00000323740.4:p.Glu173Asp
ENST00000426995.2:c.519A>C ENSP00000392143.2:p.Glu173Asp
NM_003356.3:c.519A>C NP_003347.1:p.Glu173Asp
NM_022803.2:c.519A>C NP_073714.1:p.Glu173Asp
XR_950298.1:n.1768+9718T>G
NM_003356.4:c.519A>C MANE Select NP_003347.1:p.Glu173Asp
NM_022803.3:c.519A>C NP_073714.1:p.Glu173Asp
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