Canonical Allele Identifier: CA2625793070
Gene: ESRRB HGNC NCBI

Linked Data

gnomAD v4: 14-76371274-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371274A>G , CM000676.2:g.76371274A>G GRCh38
NC_000014.8:g.76837617A>G , CM000676.1:g.76837617A>G GRCh37
NC_000014.7:g.75907370A>G NCBI36
NG_012278.1:g.4928A>G
NG_012278.2:g.4928A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000512784.6:c.2+60358A>G ENSP00000424992.2:n.2+60358A>G
ENST00000505752.5:c.-444A>G ENSP00000423004.1:n.-444A>G
ENST00000512784.5:c.2+60358A>G ENSP00000424992.1:n.2+60358A>G
NM_004452.4:c.-444A>G NP_004443.3:n.-444A>G
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