Canonical Allele Identifier: CA343473017

Gene: RXRG

Linked Data

• dbSNP Id: rs1260132672
• gnomAD v2: 1-165389215-T-A
• gnomAD v4: 1-165419978-T-A
• MyVariant Identifiers: chr1:g.165389215T>A (hg19) ; chr1:g.165419978T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419978T>A , CM000663.2:g.165419978T>A	GRCh38
NC_000001.10:g.165389215T>A , CM000663.1:g.165389215T>A	GRCh37
NC_000001.9:g.163655839T>A	NCBI36
NG_029517.1:g.30378A>T
NG_029517.2:g.30378A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.334A>T MANE Select	ENSP00000352900.5:p.Ile112Phe
ENST00000359842.9:c.334A>T	ENSP00000352900.5:p.Ile112Phe
ENST00000470566.1:n.259A>T
ENST00000619224.1:c.-36A>T	ENSP00000482458.1:n.-36A>T
NM_001256570.1:c.-36A>T	NP_001243499.1:n.-36A>T
NM_001256571.1:c.-36A>T	NP_001243500.1:n.-36A>T
NM_006917.4:c.334A>T	NP_008848.1:p.Ile112Phe
NM_006917.5:c.334A>T MANE Select	NP_008848.1:p.Ile112Phe
NM_001256571.2:c.-36A>T	NP_001243500.1:n.-36A>T
NM_001256570.2:c.-36A>T	NP_001243499.1:n.-36A>T