Canonical Allele Identifier: CA2147961559

Gene: ESRRB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76501289T= , CM000676.2:g.76501289T=	GRCh38
NC_000014.8:g.76967632T= , CM000676.1:g.76967632T=	GRCh37
NC_000014.7:g.76037385T=	NCBI36
NG_012278.1:g.134943T=
NG_012278.2:g.134943T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.*568T=	ENSP00000370270.2:n.*568T=
ENST00000644823.1:c.*2831T= MANE Select	ENSP00000493776.1:n.*2831T=
ENST00000380887.6:c.*568T=	ENSP00000370270.2:n.*568T=
ENST00000509242.5:c.*568T=	ENSP00000422488.1:n.*568T=
ENST00000611036.1:n.1644T=
NM_004452.3:c.*568T=	NP_004443.3:n.*568T=
XM_011536547.1:c.*1064T=	XP_011534849.1:n.*1064T=
XM_011536548.1:c.*1064T=	XP_011534850.1:n.*1064T=
XM_011536549.1:c.*1064T=	XP_011534851.1:n.*1064T=
XM_011536550.1:c.*1064T=	XP_011534852.1:n.*1064T=
XM_011536551.1:c.*1064T=	XP_011534853.1:n.*1064T=
XM_011536552.1:c.*1064T=	XP_011534854.1:n.*1064T=
XM_011536553.1:c.*2327T=	XP_011534855.1:n.*2327T=
XM_011536554.1:c.*568T=	XP_011534856.1:n.*568T=
XM_011536555.1:c.*1064T=	XP_011534857.1:n.*1064T=
XR_943401.1:n.2592T=
XR_944039.1:n.144+868A=
XM_011536547.2:c.*1064T=	XP_011534849.1:n.*1064T=
XM_011536550.2:c.*1064T=	XP_011534852.1:n.*1064T=
XM_011536553.2:c.*2327T=	XP_011534855.1:n.*2327T=
XM_011536554.2:c.*568T=	XP_011534856.1:n.*568T=
XM_017021085.1:c.*1064T=	XP_016876574.1:n.*1064T=
XM_024449508.1:c.*1407T=	XP_024305276.1:n.*1407T=
XM_024449509.1:c.*568T=	XP_024305277.1:n.*568T=
XR_943401.2:n.2815T=
NM_001379180.1:c.*2831T= MANE Select	NP_001366109.1:n.*2831T=
NM_004452.4:c.*568T=	NP_004443.3:n.*568T=