Canonical Allele Identifier: CA2625793231
Gene: ESRRB HGNC NCBI

Linked Data

gnomAD v4: 14-76371538-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371538T>C , CM000676.2:g.76371538T>C GRCh38
NC_000014.8:g.76837881T>C , CM000676.1:g.76837881T>C GRCh37
NC_000014.7:g.75907634T>C NCBI36
NG_012278.1:g.5192T>C
NG_012278.2:g.5192T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-180T>C ENSP00000370270.2:n.-180T>C
ENST00000505752.6:c.-180T>C ENSP00000423004.1:n.-180T>C
ENST00000512784.6:c.2+60622T>C ENSP00000424992.2:n.2+60622T>C
ENST00000505752.5:c.-180T>C ENSP00000423004.1:n.-180T>C
ENST00000512784.5:c.2+60622T>C ENSP00000424992.1:n.2+60622T>C
NM_004452.3:c.-180T>C NP_004443.3:n.-180T>C
XM_011536548.1:c.-180T>C XP_011534850.1:n.-180T>C
NM_004452.4:c.-180T>C NP_004443.3:n.-180T>C
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