Canonical Allele Identifier: CA1219980
Gene: RXRG HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.165406806T>C
GRCh37 chr1:g.165376043T>C
gnomAD v2:
1:165376043 T / C
gnomAD v3:
1:165406806 T / C
gnomAD v4:
chr1-165406806-T-C
Joint Max Group AF 0.93000837 (EAS)
Genomes Max Group AF 0.90506881 (EAS)
Exomes Max Group AF 0.93090472 (EAS)
dbSNP:
283696
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165406806T>C , CM000663.2:g.165406806T>C GRCh38
NC_000001.10:g.165376043T>C , CM000663.1:g.165376043T>C GRCh37
NC_000001.9:g.163642667T>C NCBI36
NG_029517.1:g.43550A>G
NG_029517.2:g.43550A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.1244+6A>G MANE Select ENSP00000352900.5:n.1244+6A>G
ENST00000359842.9:c.1244+6A>G ENSP00000352900.5:n.1244+6A>G
ENST00000619224.1:c.875+6A>G ENSP00000482458.1:n.875+6A>G
NM_001256570.1:c.875+6A>G NP_001243499.1:n.875+6A>G
NM_001256571.1:c.875+6A>G NP_001243500.1:n.875+6A>G
NM_006917.4:c.1244+6A>G NP_008848.1:n.1244+6A>G
NM_006917.5:c.1244+6A>G MANE Select NP_008848.1:n.1244+6A>G
NM_001256571.2:c.875+6A>G NP_001243500.1:n.875+6A>G
NM_001256570.2:c.875+6A>G NP_001243499.1:n.875+6A>G
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