Canonical Allele Identifier: CA1204419789
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439902T= , CM000663.2:g.165439902T= GRCh38
NC_000001.10:g.165409139T= , CM000663.1:g.165409139T= GRCh37
NC_000001.9:g.163675763T= NCBI36
NG_029517.1:g.10454A=
NG_029517.2:g.10454A=

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+4943A= MANE Select ENSP00000352900.5:n.49+4943A=
ENST00000359842.9:c.49+4943A= ENSP00000352900.5:n.49+4943A=
ENST00000465764.1:n.329-2701A=
ENST00000619224.1:c.-379+4943A= ENSP00000482458.1:n.-379+4943A=
NM_001256570.1:c.-379+4943A= NP_001243499.1:n.-379+4943A=
NM_006917.4:c.49+4943A= NP_008848.1:n.49+4943A=
NR_033824.1:n.512-2701A=
NM_006917.5:c.49+4943A= MANE Select NP_008848.1:n.49+4943A=
NR_033824.2:n.283-2701A=
NM_001256570.2:c.-379+4943A= NP_001243499.1:n.-379+4943A=