Canonical Allele Identifier: CA2147904119
Gene: ESRRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371503C= , CM000676.2:g.76371503C= GRCh38
NC_000014.8:g.76837846C= , CM000676.1:g.76837846C= GRCh37
NC_000014.7:g.75907599C= NCBI36
NG_012278.1:g.5157C=
NG_012278.2:g.5157C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-215C= ENSP00000370270.2:n.-215C=
ENST00000505752.6:c.-215C= ENSP00000423004.1:n.-215C=
ENST00000512784.6:c.2+60587C= ENSP00000424992.2:n.2+60587C=
ENST00000505752.5:c.-215C= ENSP00000423004.1:n.-215C=
ENST00000512784.5:c.2+60587C= ENSP00000424992.1:n.2+60587C=
NM_004452.3:c.-215C= NP_004443.3:n.-215C=
XM_011536548.1:c.-215C= XP_011534850.1:n.-215C=
NM_004452.4:c.-215C= NP_004443.3:n.-215C=