Canonical Allele Identifier: CA1146688553
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439786G= , CM000663.2:g.165439786G= GRCh38
NC_000001.10:g.165409023G= , CM000663.1:g.165409023G= GRCh37
NC_000001.9:g.163675647G= NCBI36
NG_029517.1:g.10570C=
NG_029517.2:g.10570C=

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+5059C= MANE Select ENSP00000352900.5:n.49+5059C=
ENST00000359842.9:c.49+5059C= ENSP00000352900.5:n.49+5059C=
ENST00000465764.1:n.329-2585C=
ENST00000619224.1:c.-379+5059C= ENSP00000482458.1:n.-379+5059C=
NM_001256570.1:c.-379+5059C= NP_001243499.1:n.-379+5059C=
NM_006917.4:c.49+5059C= NP_008848.1:n.49+5059C=
NR_033824.1:n.512-2585C=
NM_006917.5:c.49+5059C= MANE Select NP_008848.1:n.49+5059C=
NR_033824.2:n.283-2585C=
NM_001256570.2:c.-379+5059C= NP_001243499.1:n.-379+5059C=