Canonical Allele Identifier: CA2147904080
Gene: ESRRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371422T= , CM000676.2:g.76371422T= GRCh38
NC_000014.8:g.76837765T= , CM000676.1:g.76837765T= GRCh37
NC_000014.7:g.75907518T= NCBI36
NG_012278.1:g.5076T=
NG_012278.2:g.5076T=

Transcript Alleles

HGVS Amino-acid change
ENST00000380887.7:c.-296T= ENSP00000370270.2:n.-296T=
ENST00000505752.6:c.-296T= ENSP00000423004.1:n.-296T=
ENST00000512784.6:c.2+60506T= ENSP00000424992.2:n.2+60506T=
ENST00000505752.5:c.-296T= ENSP00000423004.1:n.-296T=
ENST00000512784.5:c.2+60506T= ENSP00000424992.1:n.2+60506T=
NM_004452.3:c.-296T= NP_004443.3:n.-296T=
XM_011536548.1:c.-296T= XP_011534850.1:n.-296T=
NM_004452.4:c.-296T= NP_004443.3:n.-296T=