Canonical Allele Identifier: CA32223408
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs528307989
gnomAD v3: 1-165439810-A-G
gnomAD v4: 1-165439810-A-G
MyVariant Identifiers: chr1:g.165409047A>G (hg19) chr1:g.165439810A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439810A>G , CM000663.2:g.165439810A>G GRCh38
NC_000001.10:g.165409047A>G , CM000663.1:g.165409047A>G GRCh37
NC_000001.9:g.163675671A>G NCBI36
NG_029517.1:g.10546T>C
NG_029517.2:g.10546T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+5035T>C MANE Select ENSP00000352900.5:n.49+5035T>C
ENST00000359842.9:c.49+5035T>C ENSP00000352900.5:n.49+5035T>C
ENST00000465764.1:n.329-2609T>C
ENST00000619224.1:c.-379+5035T>C ENSP00000482458.1:n.-379+5035T>C
NM_001256570.1:c.-379+5035T>C NP_001243499.1:n.-379+5035T>C
NM_006917.4:c.49+5035T>C NP_008848.1:n.49+5035T>C
NR_033824.1:n.512-2609T>C
NM_006917.5:c.49+5035T>C MANE Select NP_008848.1:n.49+5035T>C
NR_033824.2:n.283-2609T>C
NM_001256570.2:c.-379+5035T>C NP_001243499.1:n.-379+5035T>C
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