Canonical Allele Identifier: CA32221226
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs976132371
MyVariant Identifiers: chr1:g.165389139T>G (hg19) chr1:g.165419902T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419902T>G , CM000663.2:g.165419902T>G GRCh38
NC_000001.10:g.165389139T>G , CM000663.1:g.165389139T>G GRCh37
NC_000001.9:g.163655763T>G NCBI36
NG_029517.1:g.30454A>C
NG_029517.2:g.30454A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.410A>C MANE Select ENSP00000352900.5:p.His137Pro
ENST00000359842.9:c.410A>C ENSP00000352900.5:p.His137Pro
ENST00000470566.1:n.335A>C
ENST00000619224.1:c.41A>C ENSP00000482458.1:p.His14Pro
NM_001256570.1:c.41A>C NP_001243499.1:p.His14Pro
NM_001256571.1:c.41A>C NP_001243500.1:p.His14Pro
NM_006917.4:c.410A>C NP_008848.1:p.His137Pro
NM_006917.5:c.410A>C MANE Select NP_008848.1:p.His137Pro
NM_001256571.2:c.41A>C NP_001243500.1:p.His14Pro
NM_001256570.2:c.41A>C NP_001243499.1:p.His14Pro
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