Canonical Allele Identifier: CA32223416
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs777212745
MyVariant Identifiers: chr1:g.165409149C>G (hg19) chr1:g.165439912C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439912C>G , CM000663.2:g.165439912C>G GRCh38
NC_000001.10:g.165409149C>G , CM000663.1:g.165409149C>G GRCh37
NC_000001.9:g.163675773C>G NCBI36
NG_029517.1:g.10444G>C
NG_029517.2:g.10444G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+4933G>C MANE Select ENSP00000352900.5:n.49+4933G>C
ENST00000359842.9:c.49+4933G>C ENSP00000352900.5:n.49+4933G>C
ENST00000465764.1:n.329-2711G>C
ENST00000619224.1:c.-379+4933G>C ENSP00000482458.1:n.-379+4933G>C
NM_001256570.1:c.-379+4933G>C NP_001243499.1:n.-379+4933G>C
NM_006917.4:c.49+4933G>C NP_008848.1:n.49+4933G>C
NR_033824.1:n.512-2711G>C
NM_006917.5:c.49+4933G>C MANE Select NP_008848.1:n.49+4933G>C
NR_033824.2:n.283-2711G>C
NM_001256570.2:c.-379+4933G>C NP_001243499.1:n.-379+4933G>C
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