Canonical Allele Identifier: CA390476696

Gene: ESRRB

Linked Data

• MyVariant Identifiers: chr14:g.76928933C>A (hg19) ; chr14:g.76462590C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76462590C>A , CM000676.2:g.76462590C>A	GRCh38
NC_000014.8:g.76928933C>A , CM000676.1:g.76928933C>A	GRCh37
NC_000014.7:g.75998686C>A	NCBI36
NG_012278.1:g.96244C>A
NG_012278.2:g.96244C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380887.7:c.443C>A	ENSP00000370270.2:p.Thr148Asn
ENST00000505752.6:c.443C>A	ENSP00000423004.1:p.Thr148Asn
ENST00000512784.6:c.458C>A	ENSP00000424992.2:p.Thr153Asn
ENST00000644823.1:c.506C>A MANE Select	ENSP00000493776.1:p.Thr169Asn
ENST00000380887.6:c.443C>A	ENSP00000370270.2:p.Thr148Asn
ENST00000505752.5:c.443C>A	ENSP00000423004.1:p.Thr148Asn
ENST00000507951.5:n.551C>A
ENST00000509242.5:c.443C>A	ENSP00000422488.1:p.Thr148Asn
ENST00000509323.1:n.155C>A
ENST00000512784.5:c.458C>A	ENSP00000424992.1:p.Thr153Asn
ENST00000556177.1:c.443C>A	ENSP00000451658.1:p.Thr148Asn
NM_004452.3:c.443C>A	NP_004443.3:p.Thr148Asn
XM_005267404.2:c.506C>A	XP_005267461.1:p.Thr169Asn
XM_011536547.1:c.506C>A	XP_011534849.1:p.Thr169Asn
XM_011536548.1:c.443C>A	XP_011534850.1:p.Thr148Asn
XM_011536549.1:c.443C>A	XP_011534851.1:p.Thr148Asn
XM_011536550.1:c.443C>A	XP_011534852.1:p.Thr148Asn
XM_011536551.1:c.443C>A	XP_011534853.1:p.Thr148Asn
XM_011536552.1:c.443C>A	XP_011534854.1:p.Thr148Asn
XM_011536553.1:c.506C>A	XP_011534855.1:p.Thr169Asn
XM_011536554.1:c.506C>A	XP_011534856.1:p.Thr169Asn
XR_943401.1:n.753C>A
XM_011536547.2:c.506C>A	XP_011534849.1:p.Thr169Asn
XM_011536550.2:c.443C>A	XP_011534852.1:p.Thr148Asn
XM_011536553.2:c.506C>A	XP_011534855.1:p.Thr169Asn
XM_011536554.2:c.506C>A	XP_011534856.1:p.Thr169Asn
XM_017021085.1:c.443C>A	XP_016876574.1:p.Thr148Asn
XM_024449508.1:c.506C>A	XP_024305276.1:p.Thr169Asn
XM_024449509.1:c.443C>A	XP_024305277.1:p.Thr148Asn
XR_001750189.1:n.976C>A
XR_943401.2:n.976C>A
NM_001379180.1:c.506C>A MANE Select	NP_001366109.1:p.Thr169Asn
NM_004452.4:c.443C>A	NP_004443.3:p.Thr148Asn