Canonical Allele Identifier: CA1220232

Gene: RXRG

Linked Data

• dbSNP Id: rs186865702
• ExAC: 1:165389288 G / A
• gnomAD v2: 1-165389288-G-A
• gnomAD v3: 1-165420051-G-A
• gnomAD v4: 1-165420051-G-A
• MyVariant Identifiers: chr1:g.165389288G>A (hg19) ; chr1:g.165420051G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420051G>A , CM000663.2:g.165420051G>A	GRCh38
NC_000001.10:g.165389288G>A , CM000663.1:g.165389288G>A	GRCh37
NC_000001.9:g.163655912G>A	NCBI36
NG_029517.1:g.30305C>T
NG_029517.2:g.30305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-37C>T MANE Select	ENSP00000352900.5:n.298-37C>T
ENST00000359842.9:c.298-37C>T	ENSP00000352900.5:n.298-37C>T
ENST00000470566.1:n.223-37C>T
ENST00000619224.1:c.-72-37C>T	ENSP00000482458.1:n.-72-37C>T
NM_001256570.1:c.-72-37C>T	NP_001243499.1:n.-72-37C>T
NM_001256571.1:c.-72-37C>T	NP_001243500.1:n.-72-37C>T
NM_006917.4:c.298-37C>T	NP_008848.1:n.298-37C>T
NM_006917.5:c.298-37C>T MANE Select	NP_008848.1:n.298-37C>T
NM_001256571.2:c.-72-37C>T	NP_001243500.1:n.-72-37C>T
NM_001256570.2:c.-72-37C>T	NP_001243499.1:n.-72-37C>T