Canonical Allele Identifier: CA487194216

Gene: ESRRB

Linked Data

• MyVariant Identifiers: chr14:g.76949026C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76482683C>T , CM000676.2:g.76482683C>T	GRCh38
NC_000014.8:g.76949026C>T , CM000676.1:g.76949026C>T	GRCh37
NC_000014.7:g.76018779C>T	NCBI36
NG_012278.1:g.116337C>T
NG_012278.2:g.116337C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.711C>T	ENSP00000370270.2:p.Ile237=
ENST00000505752.6:c.711C>T	ENSP00000423004.1:p.Ile237=
ENST00000512784.6:c.726C>T	ENSP00000424992.2:p.Ile242=
ENST00000644823.1:c.774C>T MANE Select	ENSP00000493776.1:p.Ile258=
ENST00000380887.6:c.711C>T	ENSP00000370270.2:p.Ile237=
ENST00000505752.5:c.711C>T	ENSP00000423004.1:p.Ile237=
ENST00000509242.5:c.711C>T	ENSP00000422488.1:p.Ile237=
ENST00000512784.5:c.726C>T	ENSP00000424992.1:p.Ile242=
ENST00000556177.1:c.711C>T	ENSP00000451658.1:p.Ile237=
NM_004452.3:c.711C>T	NP_004443.3:p.Ile237=
XM_005267404.2:c.774C>T	XP_005267461.1:p.Ile258=
XM_011536547.1:c.774C>T	XP_011534849.1:p.Ile258=
XM_011536548.1:c.711C>T	XP_011534850.1:p.Ile237=
XM_011536549.1:c.711C>T	XP_011534851.1:p.Ile237=
XM_011536550.1:c.711C>T	XP_011534852.1:p.Ile237=
XM_011536551.1:c.711C>T	XP_011534853.1:p.Ile237=
XM_011536552.1:c.711C>T	XP_011534854.1:p.Ile237=
XM_011536553.1:c.774C>T	XP_011534855.1:p.Ile258=
XM_011536554.1:c.774C>T	XP_011534856.1:p.Ile258=
XM_011536555.1:c.33C>T	XP_011534857.1:p.Ile11=
XR_943401.1:n.1021C>T
XR_944039.1:n.145-5843G>A
XM_011536547.2:c.774C>T	XP_011534849.1:p.Ile258=
XM_011536550.2:c.711C>T	XP_011534852.1:p.Ile237=
XM_011536553.2:c.774C>T	XP_011534855.1:p.Ile258=
XM_011536554.2:c.774C>T	XP_011534856.1:p.Ile258=
XM_017021085.1:c.711C>T	XP_016876574.1:p.Ile237=
XM_024449508.1:c.774C>T	XP_024305276.1:p.Ile258=
XM_024449509.1:c.711C>T	XP_024305277.1:p.Ile237=
XR_001750189.1:n.1244C>T
XR_943401.2:n.1244C>T
NM_001379180.1:c.774C>T MANE Select	NP_001366109.1:p.Ile258=
NM_004452.4:c.711C>T	NP_004443.3:p.Ile237=