Canonical Allele Identifier: CA2147935212

Gene: ESRRB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76439405A= , CM000676.2:g.76439405A=	GRCh38
NC_000014.8:g.76905748A= , CM000676.1:g.76905748A=	GRCh37
NC_000014.7:g.75975501A=	NCBI36
NG_012278.1:g.73059A=
NG_012278.2:g.73059A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.52A=	ENSP00000370270.2:p.Thr18=
ENST00000505752.6:c.52A=	ENSP00000423004.1:p.Thr18=
ENST00000512784.6:c.67A=	ENSP00000424992.2:p.Thr23=
ENST00000644823.1:c.115A= MANE Select	ENSP00000493776.1:p.Thr39=
ENST00000380887.6:c.52A=	ENSP00000370270.2:p.Thr18=
ENST00000505752.5:c.52A=	ENSP00000423004.1:p.Thr18=
ENST00000507951.5:n.160A=
ENST00000509242.5:c.52A=	ENSP00000422488.1:p.Thr18=
ENST00000512784.5:c.67A=	ENSP00000424992.1:p.Thr23=
ENST00000556177.1:c.52A=	ENSP00000451658.1:p.Thr18=
NM_004452.3:c.52A=	NP_004443.3:p.Thr18=
XM_005267404.2:c.115A=	XP_005267461.1:p.Thr39=
XM_011536547.1:c.115A=	XP_011534849.1:p.Thr39=
XM_011536548.1:c.52A=	XP_011534850.1:p.Thr18=
XM_011536549.1:c.52A=	XP_011534851.1:p.Thr18=
XM_011536550.1:c.52A=	XP_011534852.1:p.Thr18=
XM_011536551.1:c.52A=	XP_011534853.1:p.Thr18=
XM_011536552.1:c.52A=	XP_011534854.1:p.Thr18=
XM_011536553.1:c.115A=	XP_011534855.1:p.Thr39=
XM_011536554.1:c.115A=	XP_011534856.1:p.Thr39=
XR_943401.1:n.362A=
XM_011536547.2:c.115A=	XP_011534849.1:p.Thr39=
XM_011536550.2:c.52A=	XP_011534852.1:p.Thr18=
XM_011536553.2:c.115A=	XP_011534855.1:p.Thr39=
XM_011536554.2:c.115A=	XP_011534856.1:p.Thr39=
XM_017021085.1:c.52A=	XP_016876574.1:p.Thr18=
XM_024449508.1:c.115A=	XP_024305276.1:p.Thr39=
XM_024449509.1:c.52A=	XP_024305277.1:p.Thr18=
XR_001750189.1:n.585A=
XR_943401.2:n.585A=
NM_001379180.1:c.115A= MANE Select	NP_001366109.1:p.Thr39=
NM_004452.4:c.52A=	NP_004443.3:p.Thr18=