Canonical Allele Identifier: CA2625793165
Gene: ESRRB HGNC NCBI

Linked Data

gnomAD v4: 14-76371437-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371437G>T , CM000676.2:g.76371437G>T GRCh38
NC_000014.8:g.76837780G>T , CM000676.1:g.76837780G>T GRCh37
NC_000014.7:g.75907533G>T NCBI36
NG_012278.1:g.5091G>T
NG_012278.2:g.5091G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380887.7:c.-281G>T ENSP00000370270.2:n.-281G>T
ENST00000505752.6:c.-281G>T ENSP00000423004.1:n.-281G>T
ENST00000512784.6:c.2+60521G>T ENSP00000424992.2:n.2+60521G>T
ENST00000505752.5:c.-281G>T ENSP00000423004.1:n.-281G>T
ENST00000512784.5:c.2+60521G>T ENSP00000424992.1:n.2+60521G>T
NM_004452.3:c.-281G>T NP_004443.3:n.-281G>T
XM_011536548.1:c.-281G>T XP_011534850.1:n.-281G>T
NM_004452.4:c.-281G>T NP_004443.3:n.-281G>T
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