Canonical Allele Identifier: CA2625793163
Gene: ESRRB HGNC NCBI

Linked Data

gnomAD v4: 14-76371432-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371432G>A , CM000676.2:g.76371432G>A GRCh38
NC_000014.8:g.76837775G>A , CM000676.1:g.76837775G>A GRCh37
NC_000014.7:g.75907528G>A NCBI36
NG_012278.1:g.5086G>A
NG_012278.2:g.5086G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380887.7:c.-286G>A ENSP00000370270.2:n.-286G>A
ENST00000505752.6:c.-286G>A ENSP00000423004.1:n.-286G>A
ENST00000512784.6:c.2+60516G>A ENSP00000424992.2:n.2+60516G>A
ENST00000505752.5:c.-286G>A ENSP00000423004.1:n.-286G>A
ENST00000512784.5:c.2+60516G>A ENSP00000424992.1:n.2+60516G>A
NM_004452.3:c.-286G>A NP_004443.3:n.-286G>A
XM_011536548.1:c.-286G>A XP_011534850.1:n.-286G>A
NM_004452.4:c.-286G>A NP_004443.3:n.-286G>A
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