Canonical Allele Identifier: CA2625793105

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76371323-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371323C>A , CM000676.2:g.76371323C>A	GRCh38
NC_000014.8:g.76837666C>A , CM000676.1:g.76837666C>A	GRCh37
NC_000014.7:g.75907419C>A	NCBI36
NG_012278.1:g.4977C>A
NG_012278.2:g.4977C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000512784.6:c.2+60407C>A	ENSP00000424992.2:n.2+60407C>A
ENST00000505752.5:c.-395C>A	ENSP00000423004.1:n.-395C>A
ENST00000512784.5:c.2+60407C>A	ENSP00000424992.1:n.2+60407C>A
XM_011536548.1:c.-395C>A	XP_011534850.1:n.-395C>A
NM_004452.4:c.-395C>A	NP_004443.3:n.-395C>A