Canonical Allele Identifier: CA343472849
Gene: RXRG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.165389134A>G (hg19) chr1:g.165419897A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419897A>G , CM000663.2:g.165419897A>G GRCh38
NC_000001.10:g.165389134A>G , CM000663.1:g.165389134A>G GRCh37
NC_000001.9:g.163655758A>G NCBI36
NG_029517.1:g.30459T>C
NG_029517.2:g.30459T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.415T>C MANE Select ENSP00000352900.5:p.Cys139Arg
ENST00000359842.9:c.415T>C ENSP00000352900.5:p.Cys139Arg
ENST00000470566.1:n.340T>C
ENST00000619224.1:c.46T>C ENSP00000482458.1:p.Cys16Arg
NM_001256570.1:c.46T>C NP_001243499.1:p.Cys16Arg
NM_001256571.1:c.46T>C NP_001243500.1:p.Cys16Arg
NM_006917.4:c.415T>C NP_008848.1:p.Cys139Arg
NM_006917.5:c.415T>C MANE Select NP_008848.1:p.Cys139Arg
NM_001256571.2:c.46T>C NP_001243500.1:p.Cys16Arg
NM_001256570.2:c.46T>C NP_001243499.1:p.Cys16Arg
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