Canonical Allele Identifier: CA15688163
Gene: UCP3 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.74009120G>A
GRCh37 chr11:g.73720165G>A
gnomAD v2:
11:73720165 G / A
gnomAD v3:
11:74009120 G / A
gnomAD v4:
chr11-74009120-G-A
Joint Max Group AF 0.29099019 (EAS)
Genomes Max Group AF 0.29102008 (EAS)
Exomes Max Group AF 0.17768 (MID)
dbSNP:
1800849
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74009120G>A , CM000673.2:g.74009120G>A GRCh38
NC_000011.9:g.73720165G>A , CM000673.1:g.73720165G>A GRCh37
NC_000011.8:g.73397813G>A NCBI36
NG_011515.1:g.5118C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000314032.8:c.-238C>T ENSP00000323740.4:n.-238C>T
NM_003356.3:c.-238C>T NP_003347.1:n.-238C>T
NM_022803.2:c.-238C>T NP_073714.1:n.-238C>T
XR_950298.1:n.1768+13086G>A
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