Canonical Allele Identifier: CA16493792
Gene: ESRRB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76404475T>C , CM000676.2:g.76404475T>C GRCh38
NC_000014.8:g.76870818T>C , CM000676.1:g.76870818T>C GRCh37
NC_000014.7:g.75940571T>C NCBI36
NG_012278.1:g.38129T>C
NG_012278.2:g.38129T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-68+16T>C ENSP00000370270.2:n.-68+16T>C
ENST00000505752.6:c.-68+16T>C ENSP00000423004.1:n.-68+16T>C
ENST00000512784.6:c.3-34866T>C ENSP00000424992.2:n.3-34866T>C
ENST00000644823.1:c.50+28024T>C MANE Select ENSP00000493776.1:n.50+28024T>C
ENST00000380887.6:c.-68+16T>C ENSP00000370270.2:n.-68+16T>C
ENST00000505752.5:c.-68+16T>C ENSP00000423004.1:n.-68+16T>C
ENST00000507951.5:n.95+28024T>C
ENST00000512784.5:c.3-34866T>C ENSP00000424992.1:n.3-34866T>C
NM_004452.3:c.-68+16T>C NP_004443.3:n.-68+16T>C
XM_005267404.2:c.50+28024T>C XP_005267461.1:n.50+28024T>C
XM_011536547.1:c.50+28024T>C XP_011534849.1:n.50+28024T>C
XM_011536548.1:c.-68+16T>C XP_011534850.1:n.-68+16T>C
XM_011536549.1:c.-68+16T>C XP_011534851.1:n.-68+16T>C
XM_011536550.1:c.-68+16T>C XP_011534852.1:n.-68+16T>C
XM_011536551.1:c.-68+16T>C XP_011534853.1:n.-68+16T>C
XM_011536552.1:c.-68+16T>C XP_011534854.1:n.-68+16T>C
XM_011536553.1:c.50+28024T>C XP_011534855.1:n.50+28024T>C
XM_011536554.1:c.50+28024T>C XP_011534856.1:n.50+28024T>C
XR_943401.1:n.297+28024T>C
XM_011536547.2:c.50+28024T>C XP_011534849.1:n.50+28024T>C
XM_011536550.2:c.-68+16T>C XP_011534852.1:n.-68+16T>C
XM_011536553.2:c.50+28024T>C XP_011534855.1:n.50+28024T>C
XM_011536554.2:c.50+28024T>C XP_011534856.1:n.50+28024T>C
XM_017021085.1:c.-68+16T>C XP_016876574.1:n.-68+16T>C
XM_024449508.1:c.50+28024T>C XP_024305276.1:n.50+28024T>C
XM_024449509.1:c.-68+16T>C XP_024305277.1:n.-68+16T>C
XR_001750189.1:n.520+28024T>C
XR_943401.2:n.520+28024T>C
NM_001379180.1:c.50+28024T>C MANE Select NP_001366109.1:n.50+28024T>C
NM_004452.4:c.-68+16T>C NP_004443.3:n.-68+16T>C
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