Canonical Allele Identifier: CA2147904032
Gene: ESRRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371343A= , CM000676.2:g.76371343A= GRCh38
NC_000014.8:g.76837686A= , CM000676.1:g.76837686A= GRCh37
NC_000014.7:g.75907439A= NCBI36
NG_012278.1:g.4997A=
NG_012278.2:g.4997A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000512784.6:c.2+60427A= ENSP00000424992.2:n.2+60427A=
ENST00000505752.5:c.-375A= ENSP00000423004.1:n.-375A=
ENST00000512784.5:c.2+60427A= ENSP00000424992.1:n.2+60427A=
XM_011536548.1:c.-375A= XP_011534850.1:n.-375A=
NM_004452.4:c.-375A= NP_004443.3:n.-375A=