Canonical Allele Identifier: CA708633338

Gene: ESRRB

Linked Data

• dbSNP Id: rs1448569654
• gnomAD v3: 14-76371505-T-G
• gnomAD v4: 14-76371505-T-G
• MyVariant Identifiers: chr14:g.76837848T>G (hg19) ; chr14:g.76371505T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371505T>G , CM000676.2:g.76371505T>G	GRCh38
NC_000014.8:g.76837848T>G , CM000676.1:g.76837848T>G	GRCh37
NC_000014.7:g.75907601T>G	NCBI36
NG_012278.1:g.5159T>G
NG_012278.2:g.5159T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.-213T>G	ENSP00000370270.2:n.-213T>G
ENST00000505752.6:c.-213T>G	ENSP00000423004.1:n.-213T>G
ENST00000512784.6:c.2+60589T>G	ENSP00000424992.2:n.2+60589T>G
ENST00000505752.5:c.-213T>G	ENSP00000423004.1:n.-213T>G
ENST00000512784.5:c.2+60589T>G	ENSP00000424992.1:n.2+60589T>G
NM_004452.3:c.-213T>G	NP_004443.3:n.-213T>G
XM_011536548.1:c.-213T>G	XP_011534850.1:n.-213T>G
NM_004452.4:c.-213T>G	NP_004443.3:n.-213T>G