Canonical Allele Identifier: CA2147919472

Gene: ESRRB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76400617G>T , CM000676.2:g.76400617G>T	GRCh38
NC_000014.8:g.76866960G>T , CM000676.1:g.76866960G>T	GRCh37
NC_000014.7:g.75936713G>T	NCBI36
NG_012278.1:g.34271G>T
NG_012278.2:g.34271G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001379180.1:c.50+24166G>T MANE Select	NP_001366109.1:n.50+24166G>T
ENST00000644823.1:c.50+24166G>T MANE Select	ENSP00000493776.1:n.50+24166G>T
NM_004452.3:c.-131-3779G>T	NP_004443.3:n.-131-3779G>T
NM_004452.4:c.-131-3779G>T	NP_004443.3:n.-131-3779G>T
ENST00000380887.7:c.-131-3779G>T	ENSP00000370270.2:n.-131-3779G>T
ENST00000505752.5:c.-131-3779G>T	ENSP00000423004.1:n.-131-3779G>T
ENST00000505752.6:c.-131-3779G>T	ENSP00000423004.1:n.-131-3779G>T
ENST00000507951.5:n.95+24166G>T
ENST00000512784.5:c.3-38724G>T	ENSP00000424992.1:n.3-38724G>T
ENST00000512784.6:c.3-38724G>T	ENSP00000424992.2:n.3-38724G>T
XM_005267404.2:c.50+24166G>T	XP_005267461.1:n.50+24166G>T
XM_011536547.1:c.50+24166G>T	XP_011534849.1:n.50+24166G>T
XM_011536547.2:c.50+24166G>T	XP_011534849.1:n.50+24166G>T
XM_011536548.1:c.-131-3779G>T	XP_011534850.1:n.-131-3779G>T
XM_011536549.1:c.-132+140G>T	XP_011534851.1:n.-132+140G>T
XM_011536550.1:c.-132+3172G>T	XP_011534852.1:n.-132+3172G>T
XM_011536550.2:c.-132+3172G>T	XP_011534852.1:n.-132+3172G>T
XM_011536551.1:c.-131-3779G>T	XP_011534853.1:n.-131-3779G>T
XM_011536552.1:c.-132+346G>T	XP_011534854.1:n.-132+346G>T
XM_011536553.1:c.50+24166G>T	XP_011534855.1:n.50+24166G>T
XM_011536553.2:c.50+24166G>T	XP_011534855.1:n.50+24166G>T
XM_011536554.1:c.50+24166G>T	XP_011534856.1:n.50+24166G>T
XM_011536554.2:c.50+24166G>T	XP_011534856.1:n.50+24166G>T
XM_024449508.1:c.50+24166G>T	XP_024305276.1:n.50+24166G>T
XR_001750189.1:n.520+24166G>T
XR_943401.1:n.297+24166G>T
XR_943401.2:n.520+24166G>T