Canonical Allele Identifier: CA2625798388

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76501414-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76501414C>A , CM000676.2:g.76501414C>A	GRCh38
NC_000014.8:g.76967757C>A , CM000676.1:g.76967757C>A	GRCh37
NC_000014.7:g.76037510C>A	NCBI36
NG_012278.1:g.135068C>A
NG_012278.2:g.135068C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380887.7:c.*693C>A	ENSP00000370270.2:n.*693C>A
ENST00000644823.1:c.*2956C>A MANE Select	ENSP00000493776.1:n.*2956C>A
ENST00000380887.6:c.*693C>A	ENSP00000370270.2:n.*693C>A
ENST00000509242.5:c.*693C>A	ENSP00000422488.1:n.*693C>A
ENST00000611036.1:n.1769C>A
NM_004452.3:c.*693C>A	NP_004443.3:n.*693C>A
XM_011536547.1:c.*1189C>A	XP_011534849.1:n.*1189C>A
XM_011536548.1:c.*1189C>A	XP_011534850.1:n.*1189C>A
XM_011536549.1:c.*1189C>A	XP_011534851.1:n.*1189C>A
XM_011536550.1:c.*1189C>A	XP_011534852.1:n.*1189C>A
XM_011536551.1:c.*1189C>A	XP_011534853.1:n.*1189C>A
XM_011536552.1:c.*1189C>A	XP_011534854.1:n.*1189C>A
XM_011536553.1:c.*2452C>A	XP_011534855.1:n.*2452C>A
XM_011536554.1:c.*693C>A	XP_011534856.1:n.*693C>A
XM_011536555.1:c.*1189C>A	XP_011534857.1:n.*1189C>A
XR_943401.1:n.2717C>A
XR_944039.1:n.144+743G>T
XM_011536547.2:c.*1189C>A	XP_011534849.1:n.*1189C>A
XM_011536550.2:c.*1189C>A	XP_011534852.1:n.*1189C>A
XM_011536553.2:c.*2452C>A	XP_011534855.1:n.*2452C>A
XM_011536554.2:c.*693C>A	XP_011534856.1:n.*693C>A
XM_017021085.1:c.*1189C>A	XP_016876574.1:n.*1189C>A
XM_024449508.1:c.*1532C>A	XP_024305276.1:n.*1532C>A
XM_024449509.1:c.*693C>A	XP_024305277.1:n.*693C>A
XR_943401.2:n.2940C>A
NM_001379180.1:c.*2956C>A MANE Select	NP_001366109.1:n.*2956C>A
NM_004452.4:c.*693C>A	NP_004443.3:n.*693C>A