Canonical Allele Identifier: CA2748021
Gene: ADIPOQ HGNC NCBI
ADIPOQ-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.186854564G>A
GRCh37 chr3:g.186572353G>A
Revel Score:
ENST00000412955 0.648
ENST00000320741 (MANE Select) 0.648
ENST00000444204 0.648
gnomAD v2:
3:186572353 G / A
gnomAD v3:
3:186854564 G / A
gnomAD v4:
chr3-186854564-G-A
Joint Max Group AF 0.00011346 (NFE)
Genomes Max Group AF 0.00006804 (NFE)
Exomes Max Group AF 0.00011277 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186854564G>A , CM000665.2:g.186854564G>A GRCh38
NC_000003.11:g.186572353G>A , CM000665.1:g.186572353G>A GRCh37
NC_000003.10:g.188055047G>A NCBI36
NG_021140.1:g.16891G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.595G>A (ADIPOQ) MANE Select ENSP00000320709.2:p.Gly199Ser
ENST00000320741.6:c.595G>A (ADIPOQ) ENSP00000320709.2:p.Gly199Ser
ENST00000444204.2:c.595G>A (ADIPOQ) ENSP00000389814.2:p.Gly199Ser
NM_001177800.1:c.595G>A (ADIPOQ) NP_001171271.1:p.Gly199Ser
NM_004797.3:c.595G>A (ADIPOQ) NP_004788.1:p.Gly199Ser
NR_046662.1:n.1560C>T (ADIPOQ-AS1)
XM_011513324.1:c.595G>A (ADIPOQ) XP_011511626.1:p.Gly199Ser
NR_046662.2:n.1689C>T (ADIPOQ-AS1)
NM_004797.4:c.595G>A (ADIPOQ) MANE Select NP_004788.1:p.Gly199Ser
NM_001177800.2:c.595G>A (ADIPOQ) NP_001171271.1:p.Gly199Ser
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