Canonical Allele Identifier: CA2648887566
Gene: RXRG HGNC NCBI

Linked Data

gnomAD v4: 1-165419809-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419809C>T , CM000663.2:g.165419809C>T GRCh38
NC_000001.10:g.165389046C>T , CM000663.1:g.165389046C>T GRCh37
NC_000001.9:g.163655670C>T NCBI36
NG_029517.1:g.30547G>A
NG_029517.2:g.30547G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.442+61G>A MANE Select ENSP00000352900.5:n.442+61G>A
ENST00000359842.9:c.442+61G>A ENSP00000352900.5:n.442+61G>A
ENST00000470566.1:n.367+61G>A
ENST00000619224.1:c.73+61G>A ENSP00000482458.1:n.73+61G>A
NM_001256570.1:c.73+61G>A NP_001243499.1:n.73+61G>A
NM_001256571.1:c.73+61G>A NP_001243500.1:n.73+61G>A
NM_006917.4:c.442+61G>A NP_008848.1:n.442+61G>A
NM_006917.5:c.442+61G>A MANE Select NP_008848.1:n.442+61G>A
NM_001256571.2:c.73+61G>A NP_001243500.1:n.73+61G>A
NM_001256570.2:c.73+61G>A NP_001243499.1:n.73+61G>A
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