Canonical Allele Identifier: CA2012137523
Gene: ADIPOR2 HGNC NCBI

Linked Data

dbSNP Id: rs1862140414

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1756707G>A , CM000674.2:g.1756707G>A GRCh38
NC_000012.11:g.1865873G>A , CM000674.1:g.1865873G>A GRCh37
NC_000012.10:g.1736134G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357103.5:c.171+2193G>A MANE Select ENSP00000349616.4:n.171+2193G>A
ENST00000357103.4:c.171+2193G>A ENSP00000349616.4:n.171+2193G>A
ENST00000537545.1:n.401+2193G>A
NM_024551.2:c.171+2193G>A NP_078827.2:n.171+2193G>A
XM_005253789.1:c.171+2193G>A XP_005253846.1:n.171+2193G>A
XM_006719018.1:c.171+2193G>A XP_006719081.1:n.171+2193G>A
XM_011521024.1:c.171+2193G>A XP_011519326.1:n.171+2193G>A
XM_011521025.1:c.171+2193G>A XP_011519327.1:n.171+2193G>A
XM_005253789.2:c.171+2193G>A XP_005253846.1:n.171+2193G>A
XM_006719018.2:c.171+2193G>A XP_006719081.1:n.171+2193G>A
XM_011521024.2:c.171+2193G>A XP_011519326.1:n.171+2193G>A
NM_024551.3:c.171+2193G>A MANE Select NP_078827.2:n.171+2193G>A
NM_001375363.1:c.171+2193G>A NP_001362292.1:n.171+2193G>A
NM_001375364.1:c.171+2193G>A NP_001362293.1:n.171+2193G>A
NM_001375365.1:c.171+2193G>A NP_001362294.1:n.171+2193G>A