Canonical Allele Identifier: CA2147904072
Gene: ESRRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371401T= , CM000676.2:g.76371401T= GRCh38
NC_000014.8:g.76837744T= , CM000676.1:g.76837744T= GRCh37
NC_000014.7:g.75907497T= NCBI36
NG_012278.1:g.5055T=
NG_012278.2:g.5055T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-317T= ENSP00000370270.2:n.-317T=
ENST00000505752.6:c.-317T= ENSP00000423004.1:n.-317T=
ENST00000512784.6:c.2+60485T= ENSP00000424992.2:n.2+60485T=
ENST00000505752.5:c.-317T= ENSP00000423004.1:n.-317T=
ENST00000512784.5:c.2+60485T= ENSP00000424992.1:n.2+60485T=
NM_004452.3:c.-317T= NP_004443.3:n.-317T=
XM_011536548.1:c.-317T= XP_011534850.1:n.-317T=
NM_004452.4:c.-317T= NP_004443.3:n.-317T=