Canonical Allele Identifier: CA2147904137
Gene: ESRRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371535G= , CM000676.2:g.76371535G= GRCh38
NC_000014.8:g.76837878G= , CM000676.1:g.76837878G= GRCh37
NC_000014.7:g.75907631G= NCBI36
NG_012278.1:g.5189G=
NG_012278.2:g.5189G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-183G= ENSP00000370270.2:n.-183G=
ENST00000505752.6:c.-183G= ENSP00000423004.1:n.-183G=
ENST00000512784.6:c.2+60619G= ENSP00000424992.2:n.2+60619G=
ENST00000505752.5:c.-183G= ENSP00000423004.1:n.-183G=
ENST00000512784.5:c.2+60619G= ENSP00000424992.1:n.2+60619G=
NM_004452.3:c.-183G= NP_004443.3:n.-183G=
XM_011536548.1:c.-183G= XP_011534850.1:n.-183G=
NM_004452.4:c.-183G= NP_004443.3:n.-183G=