Canonical Allele Identifier: CA2147904008
Gene: ESRRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371302A= , CM000676.2:g.76371302A= GRCh38
NC_000014.8:g.76837645A= , CM000676.1:g.76837645A= GRCh37
NC_000014.7:g.75907398A= NCBI36
NG_012278.1:g.4956A=
NG_012278.2:g.4956A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000512784.6:c.2+60386A= ENSP00000424992.2:n.2+60386A=
ENST00000505752.5:c.-416A= ENSP00000423004.1:n.-416A=
ENST00000512784.5:c.2+60386A= ENSP00000424992.1:n.2+60386A=
XM_011536548.1:c.-416A= XP_011534850.1:n.-416A=
NM_004452.4:c.-416A= NP_004443.3:n.-416A=