Canonical Allele Identifier: CA390476688

Gene: ESRRB

Linked Data

• MyVariant Identifiers: chr14:g.76928932A>G (hg19) ; chr14:g.76462589A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76462589A>G , CM000676.2:g.76462589A>G	GRCh38
NC_000014.8:g.76928932A>G , CM000676.1:g.76928932A>G	GRCh37
NC_000014.7:g.75998685A>G	NCBI36
NG_012278.1:g.96243A>G
NG_012278.2:g.96243A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380887.7:c.442A>G	ENSP00000370270.2:p.Thr148Ala
ENST00000505752.6:c.442A>G	ENSP00000423004.1:p.Thr148Ala
ENST00000512784.6:c.457A>G	ENSP00000424992.2:p.Thr153Ala
ENST00000644823.1:c.505A>G MANE Select	ENSP00000493776.1:p.Thr169Ala
ENST00000380887.6:c.442A>G	ENSP00000370270.2:p.Thr148Ala
ENST00000505752.5:c.442A>G	ENSP00000423004.1:p.Thr148Ala
ENST00000507951.5:n.550A>G
ENST00000509242.5:c.442A>G	ENSP00000422488.1:p.Thr148Ala
ENST00000509323.1:n.154A>G
ENST00000512784.5:c.457A>G	ENSP00000424992.1:p.Thr153Ala
ENST00000556177.1:c.442A>G	ENSP00000451658.1:p.Thr148Ala
NM_004452.3:c.442A>G	NP_004443.3:p.Thr148Ala
XM_005267404.2:c.505A>G	XP_005267461.1:p.Thr169Ala
XM_011536547.1:c.505A>G	XP_011534849.1:p.Thr169Ala
XM_011536548.1:c.442A>G	XP_011534850.1:p.Thr148Ala
XM_011536549.1:c.442A>G	XP_011534851.1:p.Thr148Ala
XM_011536550.1:c.442A>G	XP_011534852.1:p.Thr148Ala
XM_011536551.1:c.442A>G	XP_011534853.1:p.Thr148Ala
XM_011536552.1:c.442A>G	XP_011534854.1:p.Thr148Ala
XM_011536553.1:c.505A>G	XP_011534855.1:p.Thr169Ala
XM_011536554.1:c.505A>G	XP_011534856.1:p.Thr169Ala
XR_943401.1:n.752A>G
XM_011536547.2:c.505A>G	XP_011534849.1:p.Thr169Ala
XM_011536550.2:c.442A>G	XP_011534852.1:p.Thr148Ala
XM_011536553.2:c.505A>G	XP_011534855.1:p.Thr169Ala
XM_011536554.2:c.505A>G	XP_011534856.1:p.Thr169Ala
XM_017021085.1:c.442A>G	XP_016876574.1:p.Thr148Ala
XM_024449508.1:c.505A>G	XP_024305276.1:p.Thr169Ala
XM_024449509.1:c.442A>G	XP_024305277.1:p.Thr148Ala
XR_001750189.1:n.975A>G
XR_943401.2:n.975A>G
NM_001379180.1:c.505A>G MANE Select	NP_001366109.1:p.Thr169Ala
NM_004452.4:c.442A>G	NP_004443.3:p.Thr148Ala