Canonical Allele Identifier: CA2625793161

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76371427-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371427T>C , CM000676.2:g.76371427T>C	GRCh38
NC_000014.8:g.76837770T>C , CM000676.1:g.76837770T>C	GRCh37
NC_000014.7:g.75907523T>C	NCBI36
NG_012278.1:g.5081T>C
NG_012278.2:g.5081T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.-291T>C	ENSP00000370270.2:n.-291T>C
ENST00000505752.6:c.-291T>C	ENSP00000423004.1:n.-291T>C
ENST00000512784.6:c.2+60511T>C	ENSP00000424992.2:n.2+60511T>C
ENST00000505752.5:c.-291T>C	ENSP00000423004.1:n.-291T>C
ENST00000512784.5:c.2+60511T>C	ENSP00000424992.1:n.2+60511T>C
NM_004452.3:c.-291T>C	NP_004443.3:n.-291T>C
XM_011536548.1:c.-291T>C	XP_011534850.1:n.-291T>C
NM_004452.4:c.-291T>C	NP_004443.3:n.-291T>C