Canonical Allele Identifier: CA263757417

Gene: ESRRB

Linked Data

• dbSNP Id: rs972079075
• MyVariant Identifiers: chr14:g.76967690C>G (hg19) ; chr14:g.76501347C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76501347C>G , CM000676.2:g.76501347C>G	GRCh38
NC_000014.8:g.76967690C>G , CM000676.1:g.76967690C>G	GRCh37
NC_000014.7:g.76037443C>G	NCBI36
NG_012278.1:g.135001C>G
NG_012278.2:g.135001C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380887.7:c.*626C>G	ENSP00000370270.2:n.*626C>G
ENST00000644823.1:c.*2889C>G MANE Select	ENSP00000493776.1:n.*2889C>G
ENST00000380887.6:c.*626C>G	ENSP00000370270.2:n.*626C>G
ENST00000509242.5:c.*626C>G	ENSP00000422488.1:n.*626C>G
ENST00000611036.1:n.1702C>G
NM_004452.3:c.*626C>G	NP_004443.3:n.*626C>G
XM_011536547.1:c.*1122C>G	XP_011534849.1:n.*1122C>G
XM_011536548.1:c.*1122C>G	XP_011534850.1:n.*1122C>G
XM_011536549.1:c.*1122C>G	XP_011534851.1:n.*1122C>G
XM_011536550.1:c.*1122C>G	XP_011534852.1:n.*1122C>G
XM_011536551.1:c.*1122C>G	XP_011534853.1:n.*1122C>G
XM_011536552.1:c.*1122C>G	XP_011534854.1:n.*1122C>G
XM_011536553.1:c.*2385C>G	XP_011534855.1:n.*2385C>G
XM_011536554.1:c.*626C>G	XP_011534856.1:n.*626C>G
XM_011536555.1:c.*1122C>G	XP_011534857.1:n.*1122C>G
XR_943401.1:n.2650C>G
XR_944039.1:n.144+810G>C
XM_011536547.2:c.*1122C>G	XP_011534849.1:n.*1122C>G
XM_011536550.2:c.*1122C>G	XP_011534852.1:n.*1122C>G
XM_011536553.2:c.*2385C>G	XP_011534855.1:n.*2385C>G
XM_011536554.2:c.*626C>G	XP_011534856.1:n.*626C>G
XM_017021085.1:c.*1122C>G	XP_016876574.1:n.*1122C>G
XM_024449508.1:c.*1465C>G	XP_024305276.1:n.*1465C>G
XM_024449509.1:c.*626C>G	XP_024305277.1:n.*626C>G
XR_943401.2:n.2873C>G
NM_001379180.1:c.*2889C>G MANE Select	NP_001366109.1:n.*2889C>G
NM_004452.4:c.*626C>G	NP_004443.3:n.*626C>G