Canonical Allele Identifier: CA1204419666
Gene: RXRG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439747A= , CM000663.2:g.165439747A= GRCh38
NC_000001.10:g.165408984A= , CM000663.1:g.165408984A= GRCh37
NC_000001.9:g.163675608A= NCBI36
NG_029517.1:g.10609T=
NG_029517.2:g.10609T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.49+5098T= MANE Select ENSP00000352900.5:n.49+5098T=
ENST00000359842.9:c.49+5098T= ENSP00000352900.5:n.49+5098T=
ENST00000465764.1:n.329-2546T=
ENST00000619224.1:c.-379+5098T= ENSP00000482458.1:n.-379+5098T=
NM_001256570.1:c.-379+5098T= NP_001243499.1:n.-379+5098T=
NM_006917.4:c.49+5098T= NP_008848.1:n.49+5098T=
NR_033824.1:n.512-2546T=
NM_006917.5:c.49+5098T= MANE Select NP_008848.1:n.49+5098T=
NR_033824.2:n.283-2546T=
NM_001256570.2:c.-379+5098T= NP_001243499.1:n.-379+5098T=
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