Canonical Allele Identifier: CA2147956190

Gene: ESRRB

Linked Data

• dbSNP Id: rs1889858926

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76482761_76482778dup , CM000676.2:g.76482761_76482778dup	GRCh38
NC_000014.8:g.76949104_76949121dup , CM000676.1:g.76949104_76949121dup	GRCh37
NC_000014.7:g.76018857_76018874dup	NCBI36
NG_012278.1:g.116415_116432dup
NG_012278.2:g.116415_116432dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.787+2_787+19dup
ENST00000505752.6:c.787+2_787+19dup
ENST00000512784.6:c.802+2_802+19dup
ENST00000644823.1:c.850+2_850+19dup
ENST00000380887.6:c.787+2_787+19dup
ENST00000505752.5:c.787+2_787+19dup
ENST00000509242.5:c.787+2_787+19dup
ENST00000512784.5:c.802+2_802+19dup
ENST00000556177.1:c.787+2_787+19dup
NM_004452.3:c.787+2_787+19dup
XM_005267404.2:c.850+2_850+19dup
XM_011536547.1:c.850+2_850+19dup
XM_011536548.1:c.787+2_787+19dup
XM_011536549.1:c.787+2_787+19dup
XM_011536550.1:c.787+2_787+19dup
XM_011536551.1:c.787+2_787+19dup
XM_011536552.1:c.787+2_787+19dup
XM_011536553.1:c.850+2_850+19dup
XM_011536554.1:c.850+2_850+19dup
XM_011536555.1:c.109+2_109+19dup
XR_943401.1:n.1097+2_1097+19dup
XR_944039.1:n.145-5933_145-5916dup
XM_011536547.2:c.850+2_850+19dup
XM_011536550.2:c.787+2_787+19dup
XM_011536553.2:c.850+2_850+19dup
XM_011536554.2:c.850+2_850+19dup
XM_017021085.1:c.787+2_787+19dup
XM_024449508.1:c.850+2_850+19dup
XM_024449509.1:c.787+2_787+19dup
XR_001750189.1:n.1320+2_1320+19dup
XR_943401.2:n.1320+2_1320+19dup
NM_001379180.1:c.850+2_850+19dup
NM_004452.4:c.787+2_787+19dup