Canonical Allele Identifier: CA2147904081
Gene: ESRRB HGNC NCBI

Linked Data

dbSNP Id: rs1884622636
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371422T>C , CM000676.2:g.76371422T>C GRCh38
NC_000014.8:g.76837765T>C , CM000676.1:g.76837765T>C GRCh37
NC_000014.7:g.75907518T>C NCBI36
NG_012278.1:g.5076T>C
NG_012278.2:g.5076T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-296T>C ENSP00000370270.2:n.-296T>C
ENST00000505752.6:c.-296T>C ENSP00000423004.1:n.-296T>C
ENST00000512784.6:c.2+60506T>C ENSP00000424992.2:n.2+60506T>C
ENST00000505752.5:c.-296T>C ENSP00000423004.1:n.-296T>C
ENST00000512784.5:c.2+60506T>C ENSP00000424992.1:n.2+60506T>C
NM_004452.3:c.-296T>C NP_004443.3:n.-296T>C
XM_011536548.1:c.-296T>C XP_011534850.1:n.-296T>C
NM_004452.4:c.-296T>C NP_004443.3:n.-296T>C
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