Canonical Allele Identifier: CA264003602

Gene: ESRRB

Linked Data

• dbSNP Id: rs149144162
• gnomAD v2: 14-76837596-A-T
• gnomAD v3: 14-76371253-A-T
• gnomAD v4: 14-76371253-A-T
• MyVariant Identifiers: chr14:g.76837596A>T (hg19) ; chr14:g.76371253A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371253A>T , CM000676.2:g.76371253A>T	GRCh38
NC_000014.8:g.76837596A>T , CM000676.1:g.76837596A>T	GRCh37
NC_000014.7:g.75907349A>T	NCBI36
NG_012278.1:g.4907A>T
NG_012278.2:g.4907A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512784.6:c.2+60337A>T	ENSP00000424992.2:n.2+60337A>T
ENST00000505752.5:c.-465A>T	ENSP00000423004.1:n.-465A>T
ENST00000512784.5:c.2+60337A>T	ENSP00000424992.1:n.2+60337A>T