Canonical Allele Identifier: CA487276326

Gene: ESRRB

Linked Data

• MyVariant Identifiers: chr14:g.76957830G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76491487G>C , CM000676.2:g.76491487G>C	GRCh38
NC_000014.8:g.76957830G>C , CM000676.1:g.76957830G>C	GRCh37
NC_000014.7:g.76027583G>C	NCBI36
NG_012278.1:g.125141G>C
NG_012278.2:g.125141G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.828G>C	ENSP00000370270.2:p.Leu276=
ENST00000505752.6:c.828G>C	ENSP00000423004.1:p.Leu276=
ENST00000512784.6:c.843G>C	ENSP00000424992.2:p.Leu281=
ENST00000644823.1:c.891G>C MANE Select	ENSP00000493776.1:p.Leu297=
ENST00000380887.6:c.828G>C	ENSP00000370270.2:p.Leu276=
ENST00000505752.5:c.828G>C	ENSP00000423004.1:p.Leu276=
ENST00000509242.5:c.828G>C	ENSP00000422488.1:p.Leu276=
ENST00000512784.5:c.843G>C	ENSP00000424992.1:p.Leu281=
ENST00000556177.1:c.828G>C	ENSP00000451658.1:p.Leu276=
NM_004452.3:c.828G>C	NP_004443.3:p.Leu276=
XM_005267404.2:c.891G>C	XP_005267461.1:p.Leu297=
XM_011536547.1:c.891G>C	XP_011534849.1:p.Leu297=
XM_011536548.1:c.828G>C	XP_011534850.1:p.Leu276=
XM_011536549.1:c.828G>C	XP_011534851.1:p.Leu276=
XM_011536550.1:c.828G>C	XP_011534852.1:p.Leu276=
XM_011536551.1:c.828G>C	XP_011534853.1:p.Leu276=
XM_011536552.1:c.828G>C	XP_011534854.1:p.Leu276=
XM_011536553.1:c.891G>C	XP_011534855.1:p.Leu297=
XM_011536554.1:c.891G>C	XP_011534856.1:p.Leu297=
XM_011536555.1:c.150G>C	XP_011534857.1:p.Leu50=
XR_943401.1:n.1138G>C
XR_944039.1:n.144+10670C>G
XM_011536547.2:c.891G>C	XP_011534849.1:p.Leu297=
XM_011536550.2:c.828G>C	XP_011534852.1:p.Leu276=
XM_011536553.2:c.891G>C	XP_011534855.1:p.Leu297=
XM_011536554.2:c.891G>C	XP_011534856.1:p.Leu297=
XM_017021085.1:c.828G>C	XP_016876574.1:p.Leu276=
XM_024449508.1:c.891G>C	XP_024305276.1:p.Leu297=
XM_024449509.1:c.828G>C	XP_024305277.1:p.Leu276=
XR_001750189.1:n.1361G>C
XR_943401.2:n.1361G>C
NM_001379180.1:c.891G>C MANE Select	NP_001366109.1:p.Leu297=
NM_004452.4:c.828G>C	NP_004443.3:p.Leu276=