Canonical Allele Identifier: CA2747956
Gene: ADIPOQ HGNC NCBI
ADIPOQ-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2527928
ClinVar RCV Id: RCV004302971
dbSNP Id: rs779058354
ExAC: 3:186572015 C / T
gnomAD v2: 3-186572015-C-T
gnomAD v3: 3-186854226-C-T
gnomAD v4: 3-186854226-C-T
MyVariant Identifiers: chr3:g.186572015C>T (hg19) chr3:g.186854226C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186854226C>T , CM000665.2:g.186854226C>T GRCh38
NC_000003.11:g.186572015C>T , CM000665.1:g.186572015C>T GRCh37
NC_000003.10:g.188054709C>T NCBI36
NG_021140.1:g.16553C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.257C>T (ADIPOQ) MANE Select ENSP00000320709.2:p.Pro86Leu
ENST00000320741.6:c.257C>T (ADIPOQ) ENSP00000320709.2:p.Pro86Leu
ENST00000444204.2:c.257C>T (ADIPOQ) ENSP00000389814.2:p.Pro86Leu
NM_001177800.1:c.257C>T (ADIPOQ) NP_001171271.1:p.Pro86Leu
NM_004797.3:c.257C>T (ADIPOQ) NP_004788.1:p.Pro86Leu
NR_046662.1:n.1898G>A (ADIPOQ-AS1)
XM_011513324.1:c.257C>T (ADIPOQ) XP_011511626.1:p.Pro86Leu
NR_046662.2:n.2027G>A (ADIPOQ-AS1)
NM_004797.4:c.257C>T (ADIPOQ) MANE Select NP_004788.1:p.Pro86Leu
NM_001177800.2:c.257C>T (ADIPOQ) NP_001171271.1:p.Pro86Leu
Search 100 bp 5'
Search 100 bp 3'