Canonical Allele Identifier: CA2625793118

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76371348-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371348C>A , CM000676.2:g.76371348C>A	GRCh38
NC_000014.8:g.76837691C>A , CM000676.1:g.76837691C>A	GRCh37
NC_000014.7:g.75907444C>A	NCBI36
NG_012278.1:g.5002C>A
NG_012278.2:g.5002C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.-370C>A	ENSP00000370270.2:n.-370C>A
ENST00000512784.6:c.2+60432C>A	ENSP00000424992.2:n.2+60432C>A
ENST00000505752.5:c.-370C>A	ENSP00000423004.1:n.-370C>A
ENST00000512784.5:c.2+60432C>A	ENSP00000424992.1:n.2+60432C>A
NM_004452.3:c.-370C>A	NP_004443.3:n.-370C>A
XM_011536548.1:c.-370C>A	XP_011534850.1:n.-370C>A
NM_004452.4:c.-370C>A	NP_004443.3:n.-370C>A