Canonical Allele Identifier: CA2147961502

Gene: ESRRB

Linked Data

• dbSNP Id: rs1890646922

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76501227_76501229dup , CM000676.2:g.76501227_76501229dup	GRCh38
NC_000014.8:g.76967570_76967572dup , CM000676.1:g.76967570_76967572dup	GRCh37
NC_000014.7:g.76037323_76037325dup	NCBI36
NG_012278.1:g.134881_134883dup
NG_012278.2:g.134881_134883dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.*506_*508dup	ENSP00000370270.2:n.*506_*508dup
ENST00000644823.1:c.*2769_*2771dup MANE Select	ENSP00000493776.1:n.*2769_*2771dup
ENST00000380887.6:c.*506_*508dup	ENSP00000370270.2:n.*506_*508dup
ENST00000509242.5:c.*506_*508dup	ENSP00000422488.1:n.*506_*508dup
ENST00000611036.1:n.1582_1584dup
NM_004452.3:c.*506_*508dup	NP_004443.3:n.*506_*508dup
XM_011536547.1:c.*1002_*1004dup	XP_011534849.1:n.*1002_*1004dup
XM_011536548.1:c.*1002_*1004dup	XP_011534850.1:n.*1002_*1004dup
XM_011536549.1:c.*1002_*1004dup	XP_011534851.1:n.*1002_*1004dup
XM_011536550.1:c.*1002_*1004dup	XP_011534852.1:n.*1002_*1004dup
XM_011536551.1:c.*1002_*1004dup	XP_011534853.1:n.*1002_*1004dup
XM_011536552.1:c.*1002_*1004dup	XP_011534854.1:n.*1002_*1004dup
XM_011536553.1:c.*2265_*2267dup	XP_011534855.1:n.*2265_*2267dup
XM_011536554.1:c.*506_*508dup	XP_011534856.1:n.*506_*508dup
XM_011536555.1:c.*1002_*1004dup	XP_011534857.1:n.*1002_*1004dup
XR_943401.1:n.2530_2532dup
XR_944039.1:n.144+929_144+931dup
XM_011536547.2:c.*1002_*1004dup	XP_011534849.1:n.*1002_*1004dup
XM_011536550.2:c.*1002_*1004dup	XP_011534852.1:n.*1002_*1004dup
XM_011536553.2:c.*2265_*2267dup	XP_011534855.1:n.*2265_*2267dup
XM_011536554.2:c.*506_*508dup	XP_011534856.1:n.*506_*508dup
XM_017021085.1:c.*1002_*1004dup	XP_016876574.1:n.*1002_*1004dup
XM_024449508.1:c.*1345_*1347dup	XP_024305276.1:n.*1345_*1347dup
XM_024449509.1:c.*506_*508dup	XP_024305277.1:n.*506_*508dup
XR_943401.2:n.2753_2755dup
NM_001379180.1:c.*2769_*2771dup MANE Select	NP_001366109.1:n.*2769_*2771dup
NM_004452.4:c.*506_*508dup	NP_004443.3:n.*506_*508dup