Canonical Allele Identifier: CA16609579
Gene: ESRRB HGNC NCBI

Linked Data

ClinVar Variation Id: 402254
ClinVar RCV Id: RCV000454320
dbSNP Id: rs1060499794

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76482046G>A , CM000676.2:g.76482046G>A GRCh38
NC_000014.8:g.76948389G>A , CM000676.1:g.76948389G>A GRCh37
NC_000014.7:g.76018142G>A NCBI36
NG_012278.1:g.115700G>A
NG_012278.2:g.115700G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380887.7:c.545G>A ENSP00000370270.2:p.Arg182His
ENST00000505752.6:c.545G>A ENSP00000423004.1:p.Arg182His
ENST00000512784.6:c.560G>A ENSP00000424992.2:p.Arg187His
ENST00000644823.1:c.608G>A MANE Select ENSP00000493776.1:p.Arg203His
ENST00000380887.6:c.545G>A ENSP00000370270.2:p.Arg182His
ENST00000505752.5:c.545G>A ENSP00000423004.1:p.Arg182His
ENST00000507951.5:n.653G>A
ENST00000509242.5:c.545G>A ENSP00000422488.1:p.Arg182His
ENST00000512784.5:c.560G>A ENSP00000424992.1:p.Arg187His
ENST00000556177.1:c.545G>A ENSP00000451658.1:p.Arg182His
NM_004452.3:c.545G>A NP_004443.3:p.Arg182His
XM_005267404.2:c.608G>A XP_005267461.1:p.Arg203His
XM_011536547.1:c.608G>A XP_011534849.1:p.Arg203His
XM_011536548.1:c.545G>A XP_011534850.1:p.Arg182His
XM_011536549.1:c.545G>A XP_011534851.1:p.Arg182His
XM_011536550.1:c.545G>A XP_011534852.1:p.Arg182His
XM_011536551.1:c.545G>A XP_011534853.1:p.Arg182His
XM_011536552.1:c.545G>A XP_011534854.1:p.Arg182His
XM_011536553.1:c.608G>A XP_011534855.1:p.Arg203His
XM_011536554.1:c.608G>A XP_011534856.1:p.Arg203His
XM_011536555.1:c.-134G>A XP_011534857.1:n.-134G>A
XR_943401.1:n.855G>A
XR_944039.1:n.145-5206C>T
XM_011536547.2:c.608G>A XP_011534849.1:p.Arg203His
XM_011536550.2:c.545G>A XP_011534852.1:p.Arg182His
XM_011536553.2:c.608G>A XP_011534855.1:p.Arg203His
XM_011536554.2:c.608G>A XP_011534856.1:p.Arg203His
XM_017021085.1:c.545G>A XP_016876574.1:p.Arg182His
XM_024449508.1:c.608G>A XP_024305276.1:p.Arg203His
XM_024449509.1:c.545G>A XP_024305277.1:p.Arg182His
XR_001750189.1:n.1078G>A
XR_943401.2:n.1078G>A
NM_001379180.1:c.608G>A MANE Select NP_001366109.1:p.Arg203His
NM_004452.4:c.545G>A NP_004443.3:p.Arg182His