Canonical Allele Identifier: CA421567702
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs1658258587
gnomAD v4: 1-165419994-G-T
MyVariant Identifiers: chr1:g.165389231G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419994G>T , CM000663.2:g.165419994G>T GRCh38
NC_000001.10:g.165389231G>T , CM000663.1:g.165389231G>T GRCh37
NC_000001.9:g.163655855G>T NCBI36
NG_029517.1:g.30362C>A
NG_029517.2:g.30362C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.318C>A MANE Select ENSP00000352900.5:p.Val106=
ENST00000359842.9:c.318C>A ENSP00000352900.5:p.Val106=
ENST00000470566.1:n.243C>A
ENST00000619224.1:c.-52C>A ENSP00000482458.1:n.-52C>A
NM_001256570.1:c.-52C>A NP_001243499.1:n.-52C>A
NM_001256571.1:c.-52C>A NP_001243500.1:n.-52C>A
NM_006917.4:c.318C>A NP_008848.1:p.Val106=
NM_006917.5:c.318C>A MANE Select NP_008848.1:p.Val106=
NM_001256571.2:c.-52C>A NP_001243500.1:n.-52C>A
NM_001256570.2:c.-52C>A NP_001243499.1:n.-52C>A
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