Canonical Allele Identifier: CA1204419788
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs1658927534
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439898G>T , CM000663.2:g.165439898G>T GRCh38
NC_000001.10:g.165409135G>T , CM000663.1:g.165409135G>T GRCh37
NC_000001.9:g.163675759G>T NCBI36
NG_029517.1:g.10458C>A
NG_029517.2:g.10458C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+4947C>A MANE Select ENSP00000352900.5:n.49+4947C>A
ENST00000359842.9:c.49+4947C>A ENSP00000352900.5:n.49+4947C>A
ENST00000465764.1:n.329-2697C>A
ENST00000619224.1:c.-379+4947C>A ENSP00000482458.1:n.-379+4947C>A
NM_001256570.1:c.-379+4947C>A NP_001243499.1:n.-379+4947C>A
NM_006917.4:c.49+4947C>A NP_008848.1:n.49+4947C>A
NR_033824.1:n.512-2697C>A
NM_006917.5:c.49+4947C>A MANE Select NP_008848.1:n.49+4947C>A
NR_033824.2:n.283-2697C>A
NM_001256570.2:c.-379+4947C>A NP_001243499.1:n.-379+4947C>A
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