Canonical Allele Identifier: CA1220185

Gene: RXRG

Linked Data

• dbSNP Id: rs766370742
• ExAC: 1:165389060 C / A
• gnomAD v2: 1-165389060-C-A
• gnomAD v4: 1-165419823-C-A
• MyVariant Identifiers: chr1:g.165389060C>A (hg19) ; chr1:g.165419823C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419823C>A , CM000663.2:g.165419823C>A	GRCh38
NC_000001.10:g.165389060C>A , CM000663.1:g.165389060C>A	GRCh37
NC_000001.9:g.163655684C>A	NCBI36
NG_029517.1:g.30533G>T
NG_029517.2:g.30533G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+47G>T MANE Select	ENSP00000352900.5:n.442+47G>T
ENST00000359842.9:c.442+47G>T	ENSP00000352900.5:n.442+47G>T
ENST00000470566.1:n.367+47G>T
ENST00000619224.1:c.73+47G>T	ENSP00000482458.1:n.73+47G>T
NM_001256570.1:c.73+47G>T	NP_001243499.1:n.73+47G>T
NM_001256571.1:c.73+47G>T	NP_001243500.1:n.73+47G>T
NM_006917.4:c.442+47G>T	NP_008848.1:n.442+47G>T
NM_006917.5:c.442+47G>T MANE Select	NP_008848.1:n.442+47G>T
NM_001256571.2:c.73+47G>T	NP_001243500.1:n.73+47G>T
NM_001256570.2:c.73+47G>T	NP_001243499.1:n.73+47G>T