Canonical Allele Identifier: CA2625793115

Gene: ESRRB

Linked Data

• gnomAD v4: 14-76371342-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371342C>T , CM000676.2:g.76371342C>T	GRCh38
NC_000014.8:g.76837685C>T , CM000676.1:g.76837685C>T	GRCh37
NC_000014.7:g.75907438C>T	NCBI36
NG_012278.1:g.4996C>T
NG_012278.2:g.4996C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000512784.6:c.2+60426C>T	ENSP00000424992.2:n.2+60426C>T
ENST00000505752.5:c.-376C>T	ENSP00000423004.1:n.-376C>T
ENST00000512784.5:c.2+60426C>T	ENSP00000424992.1:n.2+60426C>T
XM_011536548.1:c.-376C>T	XP_011534850.1:n.-376C>T
NM_004452.4:c.-376C>T	NP_004443.3:n.-376C>T