Canonical Allele Identifier: CA2554412050
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439790C>A , CM000663.2:g.165439790C>A GRCh38
NC_000001.10:g.165409027C>A , CM000663.1:g.165409027C>A GRCh37
NC_000001.9:g.163675651C>A NCBI36
NG_029517.1:g.10566G>T
NG_029517.2:g.10566G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+5055G>T MANE Select ENSP00000352900.5:n.49+5055G>T
ENST00000359842.9:c.49+5055G>T ENSP00000352900.5:n.49+5055G>T
ENST00000465764.1:n.329-2589G>T
ENST00000619224.1:c.-379+5055G>T ENSP00000482458.1:n.-379+5055G>T
NM_001256570.1:c.-379+5055G>T NP_001243499.1:n.-379+5055G>T
NM_006917.4:c.49+5055G>T NP_008848.1:n.49+5055G>T
NR_033824.1:n.512-2589G>T
NM_006917.5:c.49+5055G>T MANE Select NP_008848.1:n.49+5055G>T
NR_033824.2:n.283-2589G>T
NM_001256570.2:c.-379+5055G>T NP_001243499.1:n.-379+5055G>T