Canonical Allele Identifier: CA15277262
Gene: ADIPOQ HGNC NCBI
ADIPOQ-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.186853407A>G
GRCh37 chr3:g.186571196A>G
gnomAD v2:
3:186571196 A / G
gnomAD v3:
3:186853407 A / G
gnomAD v4:
chr3-186853407-A-G
Joint Max Group AF 0.28729809 (EAS)
Genomes Max Group AF 0.27849443 (EAS)
Exomes Max Group AF 0.28713159 (EAS)
dbSNP:
2241767
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186853407A>G , CM000665.2:g.186853407A>G GRCh38
NC_000003.11:g.186571196A>G , CM000665.1:g.186571196A>G GRCh37
NC_000003.10:g.188053890A>G NCBI36
NG_021140.1:g.15734A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.214+135A>G (ADIPOQ) MANE Select ENSP00000320709.2:n.214+135A>G
ENST00000320741.6:c.214+135A>G (ADIPOQ) ENSP00000320709.2:n.214+135A>G
ENST00000444204.2:c.214+135A>G (ADIPOQ) ENSP00000389814.2:n.214+135A>G
NM_001177800.1:c.214+135A>G (ADIPOQ) NP_001171271.1:n.214+135A>G
NM_004797.3:c.214+135A>G (ADIPOQ) NP_004788.1:n.214+135A>G
NR_046662.1:n.2087-165T>C (ADIPOQ-AS1)
XM_011513324.1:c.214+135A>G (ADIPOQ) XP_011511626.1:n.214+135A>G
NR_046662.2:n.2216-165T>C (ADIPOQ-AS1)
NM_004797.4:c.214+135A>G (ADIPOQ) MANE Select NP_004788.1:n.214+135A>G
NM_001177800.2:c.214+135A>G (ADIPOQ) NP_001171271.1:n.214+135A>G
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