Canonical Allele Identifier: CA2147904153

Gene: ESRRB

Linked Data

• dbSNP Id: rs1884626143

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371572del , CM000676.2:g.76371572del	GRCh38
NC_000014.8:g.76837915del , CM000676.1:g.76837915del	GRCh37
NC_000014.7:g.75907668del	NCBI36
NG_012278.1:g.5226del
NG_012278.2:g.5226del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.-146del	ENSP00000370270.2:n.-146del
ENST00000505752.6:c.-146del	ENSP00000423004.1:n.-146del
ENST00000512784.6:c.2+60656del	ENSP00000424992.2:n.2+60656del
ENST00000505752.5:c.-146del	ENSP00000423004.1:n.-146del
ENST00000512784.5:c.2+60656del	ENSP00000424992.1:n.2+60656del
NM_004452.3:c.-146del	NP_004443.3:n.-146del
XM_011536548.1:c.-146del	XP_011534850.1:n.-146del
NM_004452.4:c.-146del	NP_004443.3:n.-146del