Canonical Allele Identifier: CA2730078469

Gene: ESRRB

Linked Data

• dbSNP Id: rs2139781364

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371329T>A , CM000676.2:g.76371329T>A	GRCh38
NC_000014.8:g.76837672T>A , CM000676.1:g.76837672T>A	GRCh37
NC_000014.7:g.75907425T>A	NCBI36
NG_012278.1:g.4983T>A
NG_012278.2:g.4983T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512784.6:c.2+60413T>A	ENSP00000424992.2:n.2+60413T>A
ENST00000505752.5:c.-389T>A	ENSP00000423004.1:n.-389T>A
ENST00000512784.5:c.2+60413T>A	ENSP00000424992.1:n.2+60413T>A
XM_011536548.1:c.-389T>A	XP_011534850.1:n.-389T>A
NM_004452.4:c.-389T>A	NP_004443.3:n.-389T>A