Canonical Allele Identifier: CA2746476417
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439733G>T , CM000663.2:g.165439733G>T GRCh38
NC_000001.10:g.165408970G>T , CM000663.1:g.165408970G>T GRCh37
NC_000001.9:g.163675594G>T NCBI36
NG_029517.1:g.10623C>A
NG_029517.2:g.10623C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.49+5112C>A MANE Select ENSP00000352900.5:n.49+5112C>A
ENST00000359842.9:c.49+5112C>A ENSP00000352900.5:n.49+5112C>A
ENST00000465764.1:n.329-2532C>A
ENST00000619224.1:c.-379+5112C>A ENSP00000482458.1:n.-379+5112C>A
NM_001256570.1:c.-379+5112C>A NP_001243499.1:n.-379+5112C>A
NM_006917.4:c.49+5112C>A NP_008848.1:n.49+5112C>A
NR_033824.1:n.512-2532C>A
NM_006917.5:c.49+5112C>A MANE Select NP_008848.1:n.49+5112C>A
NR_033824.2:n.283-2532C>A
NM_001256570.2:c.-379+5112C>A NP_001243499.1:n.-379+5112C>A