Canonical Allele Identifier: CA708633157
Gene: ESRRB HGNC NCBI

Linked Data

dbSNP Id: rs1309175275
gnomAD v3: 14-76371344-G-A
gnomAD v4: 14-76371344-G-A
MyVariant Identifiers: chr14:g.76837687G>A (hg19) chr14:g.76371344G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371344G>A , CM000676.2:g.76371344G>A GRCh38
NC_000014.8:g.76837687G>A , CM000676.1:g.76837687G>A GRCh37
NC_000014.7:g.75907440G>A NCBI36
NG_012278.1:g.4998G>A
NG_012278.2:g.4998G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000512784.6:c.2+60428G>A ENSP00000424992.2:n.2+60428G>A
ENST00000505752.5:c.-374G>A ENSP00000423004.1:n.-374G>A
ENST00000512784.5:c.2+60428G>A ENSP00000424992.1:n.2+60428G>A
XM_011536548.1:c.-374G>A XP_011534850.1:n.-374G>A
NM_004452.4:c.-374G>A NP_004443.3:n.-374G>A
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