Canonical Allele Identifier: CA2147904028

Gene: ESRRB

Linked Data

• dbSNP Id: rs1566862939

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371337G>A , CM000676.2:g.76371337G>A	GRCh38
NC_000014.8:g.76837680G>A , CM000676.1:g.76837680G>A	GRCh37
NC_000014.7:g.75907433G>A	NCBI36
NG_012278.1:g.4991G>A
NG_012278.2:g.4991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512784.6:c.2+60421G>A	ENSP00000424992.2:n.2+60421G>A
ENST00000505752.5:c.-381G>A	ENSP00000423004.1:n.-381G>A
ENST00000512784.5:c.2+60421G>A	ENSP00000424992.1:n.2+60421G>A
XM_011536548.1:c.-381G>A	XP_011534850.1:n.-381G>A
NM_004452.4:c.-381G>A	NP_004443.3:n.-381G>A