Canonical Allele Identifier: CA263741419

Gene: ESRRB

Linked Data

• ClinVar Variation Id: 1208462
• ClinVar RCV Id: RCV001576800
• dbSNP Id: rs113562033
• gnomAD v2: 14-76949157-C-T
• gnomAD v3: 14-76482814-C-T
• gnomAD v4: 14-76482814-C-T
• MyVariant Identifiers: chr14:g.76949157C>T (hg19) ; chr14:g.76482814C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76482814C>T , CM000676.2:g.76482814C>T	GRCh38
NC_000014.8:g.76949157C>T , CM000676.1:g.76949157C>T	GRCh37
NC_000014.7:g.76018910C>T	NCBI36
NG_012278.1:g.116468C>T
NG_012278.2:g.116468C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.787+55C>T	ENSP00000370270.2:n.787+55C>T
ENST00000505752.6:c.787+55C>T	ENSP00000423004.1:n.787+55C>T
ENST00000512784.6:c.802+55C>T	ENSP00000424992.2:n.802+55C>T
ENST00000644823.1:c.850+55C>T MANE Select	ENSP00000493776.1:n.850+55C>T
ENST00000380887.6:c.787+55C>T	ENSP00000370270.2:n.787+55C>T
ENST00000505752.5:c.787+55C>T	ENSP00000423004.1:n.787+55C>T
ENST00000509242.5:c.787+55C>T	ENSP00000422488.1:n.787+55C>T
ENST00000512784.5:c.802+55C>T	ENSP00000424992.1:n.802+55C>T
ENST00000556177.1:c.787+55C>T	ENSP00000451658.1:n.787+55C>T
NM_004452.3:c.787+55C>T	NP_004443.3:n.787+55C>T
XM_005267404.2:c.850+55C>T	XP_005267461.1:n.850+55C>T
XM_011536547.1:c.850+55C>T	XP_011534849.1:n.850+55C>T
XM_011536548.1:c.787+55C>T	XP_011534850.1:n.787+55C>T
XM_011536549.1:c.787+55C>T	XP_011534851.1:n.787+55C>T
XM_011536550.1:c.787+55C>T	XP_011534852.1:n.787+55C>T
XM_011536551.1:c.787+55C>T	XP_011534853.1:n.787+55C>T
XM_011536552.1:c.787+55C>T	XP_011534854.1:n.787+55C>T
XM_011536553.1:c.850+55C>T	XP_011534855.1:n.850+55C>T
XM_011536554.1:c.850+55C>T	XP_011534856.1:n.850+55C>T
XM_011536555.1:c.109+55C>T	XP_011534857.1:n.109+55C>T
XR_943401.1:n.1097+55C>T
XR_944039.1:n.145-5974G>A
XM_011536547.2:c.850+55C>T	XP_011534849.1:n.850+55C>T
XM_011536550.2:c.787+55C>T	XP_011534852.1:n.787+55C>T
XM_011536553.2:c.850+55C>T	XP_011534855.1:n.850+55C>T
XM_011536554.2:c.850+55C>T	XP_011534856.1:n.850+55C>T
XM_017021085.1:c.787+55C>T	XP_016876574.1:n.787+55C>T
XM_024449508.1:c.850+55C>T	XP_024305276.1:n.850+55C>T
XM_024449509.1:c.787+55C>T	XP_024305277.1:n.787+55C>T
XR_001750189.1:n.1320+55C>T
XR_943401.2:n.1320+55C>T
NM_001379180.1:c.850+55C>T MANE Select	NP_001366109.1:n.850+55C>T
NM_004452.4:c.787+55C>T	NP_004443.3:n.787+55C>T