Canonical Allele Identifier: CA32221237

Gene: RXRG

Linked Data

• dbSNP Id: rs769987464
• gnomAD v4: 1-165420153-C-T
• MyVariant Identifiers: chr1:g.165389390C>T (hg19) ; chr1:g.165420153C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420153C>T , CM000663.2:g.165420153C>T	GRCh38
NC_000001.10:g.165389390C>T , CM000663.1:g.165389390C>T	GRCh37
NC_000001.9:g.163656014C>T	NCBI36
NG_029517.1:g.30203G>A
NG_029517.2:g.30203G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-139G>A MANE Select	ENSP00000352900.5:n.298-139G>A
ENST00000359842.9:c.298-139G>A	ENSP00000352900.5:n.298-139G>A
ENST00000470566.1:n.223-139G>A
ENST00000619224.1:c.-72-139G>A	ENSP00000482458.1:n.-72-139G>A
NM_001256570.1:c.-72-139G>A	NP_001243499.1:n.-72-139G>A
NM_001256571.1:c.-72-139G>A	NP_001243500.1:n.-72-139G>A
NM_006917.4:c.298-139G>A	NP_008848.1:n.298-139G>A
NM_006917.5:c.298-139G>A MANE Select	NP_008848.1:n.298-139G>A
NM_001256571.2:c.-72-139G>A	NP_001243500.1:n.-72-139G>A
NM_001256570.2:c.-72-139G>A	NP_001243499.1:n.-72-139G>A