Canonical Allele Identifier: CA390479085
Gene: ESRRB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76491586G>T , CM000676.2:g.76491586G>T GRCh38
NC_000014.8:g.76957929G>T , CM000676.1:g.76957929G>T GRCh37
NC_000014.7:g.76027682G>T NCBI36
NG_012278.1:g.125240G>T
NG_012278.2:g.125240G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380887.7:c.927G>T ENSP00000370270.2:p.Glu309Asp
ENST00000505752.6:c.927G>T ENSP00000423004.1:p.Glu309Asp
ENST00000512784.6:c.942G>T ENSP00000424992.2:p.Glu314Asp
ENST00000644823.1:c.990G>T MANE Select ENSP00000493776.1:p.Glu330Asp
ENST00000380887.6:c.927G>T ENSP00000370270.2:p.Glu309Asp
ENST00000505752.5:c.927G>T ENSP00000423004.1:p.Glu309Asp
ENST00000509242.5:c.927G>T ENSP00000422488.1:p.Glu309Asp
ENST00000512784.5:c.942G>T ENSP00000424992.1:p.Glu314Asp
ENST00000556177.1:c.927G>T ENSP00000451658.1:p.Glu309Asp
NM_004452.3:c.927G>T NP_004443.3:p.Glu309Asp
XM_005267404.2:c.990G>T XP_005267461.1:p.Glu330Asp
XM_011536547.1:c.990G>T XP_011534849.1:p.Glu330Asp
XM_011536548.1:c.927G>T XP_011534850.1:p.Glu309Asp
XM_011536549.1:c.927G>T XP_011534851.1:p.Glu309Asp
XM_011536550.1:c.927G>T XP_011534852.1:p.Glu309Asp
XM_011536551.1:c.927G>T XP_011534853.1:p.Glu309Asp
XM_011536552.1:c.927G>T XP_011534854.1:p.Glu309Asp
XM_011536553.1:c.990G>T XP_011534855.1:p.Glu330Asp
XM_011536554.1:c.990G>T XP_011534856.1:p.Glu330Asp
XM_011536555.1:c.249G>T XP_011534857.1:p.Glu83Asp
XR_943401.1:n.1237G>T
XR_944039.1:n.144+10571C>A
XM_011536547.2:c.990G>T XP_011534849.1:p.Glu330Asp
XM_011536550.2:c.927G>T XP_011534852.1:p.Glu309Asp
XM_011536553.2:c.990G>T XP_011534855.1:p.Glu330Asp
XM_011536554.2:c.990G>T XP_011534856.1:p.Glu330Asp
XM_017021085.1:c.927G>T XP_016876574.1:p.Glu309Asp
XM_024449508.1:c.990G>T XP_024305276.1:p.Glu330Asp
XM_024449509.1:c.927G>T XP_024305277.1:p.Glu309Asp
XR_001750189.1:n.1460G>T
XR_943401.2:n.1460G>T
NM_001379180.1:c.990G>T MANE Select NP_001366109.1:p.Glu330Asp
NM_004452.4:c.927G>T NP_004443.3:p.Glu309Asp