Canonical Allele Identifier: CA15261591
Gene: ADIPOQ HGNC NCBI
ADIPOQ-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.186853334G>T
GRCh37 chr3:g.186571123G>T
gnomAD v2:
3:186571123 G / T
gnomAD v3:
3:186853334 G / T
gnomAD v4:
chr3-186853334-G-T
Joint Max Group AF 0.35816729 (AFR)
Genomes Max Group AF 0.35484334 (AFR)
Exomes Max Group AF 0.35910133 (AFR)
dbSNP:
1501299
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186853334G>T , CM000665.2:g.186853334G>T GRCh38
NC_000003.11:g.186571123G>T , CM000665.1:g.186571123G>T GRCh37
NC_000003.10:g.188053817G>T NCBI36
NG_021140.1:g.15661G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.214+62G>T (ADIPOQ) MANE Select ENSP00000320709.2:n.214+62G>T
ENST00000320741.6:c.214+62G>T (ADIPOQ) ENSP00000320709.2:n.214+62G>T
ENST00000444204.2:c.214+62G>T (ADIPOQ) ENSP00000389814.2:n.214+62G>T
NM_001177800.1:c.214+62G>T (ADIPOQ) NP_001171271.1:n.214+62G>T
NM_004797.3:c.214+62G>T (ADIPOQ) NP_004788.1:n.214+62G>T
NR_046662.1:n.2087-92C>A (ADIPOQ-AS1)
XM_011513324.1:c.214+62G>T (ADIPOQ) XP_011511626.1:n.214+62G>T
NR_046662.2:n.2216-92C>A (ADIPOQ-AS1)
NM_004797.4:c.214+62G>T (ADIPOQ) MANE Select NP_004788.1:n.214+62G>T
NM_001177800.2:c.214+62G>T (ADIPOQ) NP_001171271.1:n.214+62G>T
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