Canonical Allele Identifier: CA708633237

Gene: ESRRB

Linked Data

• dbSNP Id: rs1262757963
• gnomAD v3: 14-76371417-CA-C
• gnomAD v4: 14-76371417-CA-C
• MyVariant Identifiers: chr14:g.76837761del (hg19) ; chr14:g.76371418del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371418del , CM000676.2:g.76371418del	GRCh38
NC_000014.8:g.76837761del , CM000676.1:g.76837761del	GRCh37
NC_000014.7:g.75907514del	NCBI36
NG_012278.1:g.5072del
NG_012278.2:g.5072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380887.7:c.-300del	ENSP00000370270.2:n.-300del
ENST00000505752.6:c.-300del	ENSP00000423004.1:n.-300del
ENST00000512784.6:c.2+60502del	ENSP00000424992.2:n.2+60502del
ENST00000505752.5:c.-300del	ENSP00000423004.1:n.-300del
ENST00000512784.5:c.2+60502del	ENSP00000424992.1:n.2+60502del
NM_004452.3:c.-300del	NP_004443.3:n.-300del
XM_011536548.1:c.-300del	XP_011534850.1:n.-300del
NM_004452.4:c.-300del	NP_004443.3:n.-300del