Canonical Allele Identifier: CA2625798154

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76501246-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76501246G>T , CM000676.2:g.76501246G>T	GRCh38
NC_000014.8:g.76967589G>T , CM000676.1:g.76967589G>T	GRCh37
NC_000014.7:g.76037342G>T	NCBI36
NG_012278.1:g.134900G>T
NG_012278.2:g.134900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.*525G>T	ENSP00000370270.2:n.*525G>T
ENST00000644823.1:c.*2788G>T MANE Select	ENSP00000493776.1:n.*2788G>T
ENST00000380887.6:c.*525G>T	ENSP00000370270.2:n.*525G>T
ENST00000509242.5:c.*525G>T	ENSP00000422488.1:n.*525G>T
ENST00000611036.1:n.1601G>T
NM_004452.3:c.*525G>T	NP_004443.3:n.*525G>T
XM_011536547.1:c.*1021G>T	XP_011534849.1:n.*1021G>T
XM_011536548.1:c.*1021G>T	XP_011534850.1:n.*1021G>T
XM_011536549.1:c.*1021G>T	XP_011534851.1:n.*1021G>T
XM_011536550.1:c.*1021G>T	XP_011534852.1:n.*1021G>T
XM_011536551.1:c.*1021G>T	XP_011534853.1:n.*1021G>T
XM_011536552.1:c.*1021G>T	XP_011534854.1:n.*1021G>T
XM_011536553.1:c.*2284G>T	XP_011534855.1:n.*2284G>T
XM_011536554.1:c.*525G>T	XP_011534856.1:n.*525G>T
XM_011536555.1:c.*1021G>T	XP_011534857.1:n.*1021G>T
XR_943401.1:n.2549G>T
XR_944039.1:n.144+911C>A
XM_011536547.2:c.*1021G>T	XP_011534849.1:n.*1021G>T
XM_011536550.2:c.*1021G>T	XP_011534852.1:n.*1021G>T
XM_011536553.2:c.*2284G>T	XP_011534855.1:n.*2284G>T
XM_011536554.2:c.*525G>T	XP_011534856.1:n.*525G>T
XM_017021085.1:c.*1021G>T	XP_016876574.1:n.*1021G>T
XM_024449508.1:c.*1364G>T	XP_024305276.1:n.*1364G>T
XM_024449509.1:c.*525G>T	XP_024305277.1:n.*525G>T
XR_943401.2:n.2772G>T
NM_001379180.1:c.*2788G>T MANE Select	NP_001366109.1:n.*2788G>T
NM_004452.4:c.*525G>T	NP_004443.3:n.*525G>T