Canonical Allele Identifier: CA2147904041
Gene: ESRRB HGNC NCBI

Linked Data

dbSNP Id: rs111446027
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371349G>C , CM000676.2:g.76371349G>C GRCh38
NC_000014.8:g.76837692G>C , CM000676.1:g.76837692G>C GRCh37
NC_000014.7:g.75907445G>C NCBI36
NG_012278.1:g.5003G>C
NG_012278.2:g.5003G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-369G>C ENSP00000370270.2:n.-369G>C
ENST00000512784.6:c.2+60433G>C ENSP00000424992.2:n.2+60433G>C
ENST00000505752.5:c.-369G>C ENSP00000423004.1:n.-369G>C
ENST00000512784.5:c.2+60433G>C ENSP00000424992.1:n.2+60433G>C
NM_004452.3:c.-369G>C NP_004443.3:n.-369G>C
XM_011536548.1:c.-369G>C XP_011534850.1:n.-369G>C
NM_004452.4:c.-369G>C NP_004443.3:n.-369G>C
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