Canonical Allele Identifier: CA89669356
Gene: ADIPOQ HGNC NCBI

Linked Data

dbSNP Id: rs983886190
MyVariant Identifiers: chr3:g.186560640A>G (hg19) chr3:g.186842851A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186842851A>G , CM000665.2:g.186842851A>G GRCh38
NC_000003.11:g.186560640A>G , CM000665.1:g.186560640A>G GRCh37
NC_000003.10:g.188043334A>G NCBI36
NG_021140.1:g.5178A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.-9+102A>G MANE Select ENSP00000320709.2:n.-9+102A>G
ENST00000320741.6:c.-9+102A>G ENSP00000320709.2:n.-9+102A>G
ENST00000444204.2:c.-60+102A>G ENSP00000389814.2:n.-60+102A>G
NM_001177800.1:c.-60+102A>G NP_001171271.1:n.-60+102A>G
NM_004797.3:c.-9+102A>G NP_004788.1:n.-9+102A>G
XM_011513324.1:c.-125+102A>G XP_011511626.1:n.-125+102A>G
NM_004797.4:c.-9+102A>G MANE Select NP_004788.1:n.-9+102A>G
NM_001177800.2:c.-60+102A>G NP_001171271.1:n.-60+102A>G
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