Canonical Allele Identifier: CA343472967

Gene: RXRG

Linked Data

• gnomAD v4: 1-165419953-C-T
• MyVariant Identifiers: chr1:g.165389190C>T (hg19) ; chr1:g.165419953C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419953C>T , CM000663.2:g.165419953C>T	GRCh38
NC_000001.10:g.165389190C>T , CM000663.1:g.165389190C>T	GRCh37
NC_000001.9:g.163655814C>T	NCBI36
NG_029517.1:g.30403G>A
NG_029517.2:g.30403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.359G>A MANE Select	ENSP00000352900.5:p.Gly120Glu
ENST00000359842.9:c.359G>A	ENSP00000352900.5:p.Gly120Glu
ENST00000470566.1:n.284G>A
ENST00000619224.1:c.-11G>A	ENSP00000482458.1:n.-11G>A
NM_001256570.1:c.-11G>A	NP_001243499.1:n.-11G>A
NM_001256571.1:c.-11G>A	NP_001243500.1:n.-11G>A
NM_006917.4:c.359G>A	NP_008848.1:p.Gly120Glu
NM_006917.5:c.359G>A MANE Select	NP_008848.1:p.Gly120Glu
NM_001256571.2:c.-11G>A	NP_001243500.1:n.-11G>A
NM_001256570.2:c.-11G>A	NP_001243499.1:n.-11G>A