Canonical Allele Identifier: CA264003604

Gene: ESRRB

Linked Data

• dbSNP Id: rs1011002174
• gnomAD v3: 14-76371272-C-A
• gnomAD v4: 14-76371272-C-A
• MyVariant Identifiers: chr14:g.76837615C>A (hg19) ; chr14:g.76371272C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.76371272C>A , CM000676.2:g.76371272C>A	GRCh38
NC_000014.8:g.76837615C>A , CM000676.1:g.76837615C>A	GRCh37
NC_000014.7:g.75907368C>A	NCBI36
NG_012278.1:g.4926C>A
NG_012278.2:g.4926C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000512784.6:c.2+60356C>A	ENSP00000424992.2:n.2+60356C>A
ENST00000505752.5:c.-446C>A	ENSP00000423004.1:n.-446C>A
ENST00000512784.5:c.2+60356C>A	ENSP00000424992.1:n.2+60356C>A
NM_004452.4:c.-446C>A	NP_004443.3:n.-446C>A