Canonical Allele Identifier: CA1008685353
Gene: RXRG HGNC NCBI

Linked Data

gnomAD v3: 1-165439867-C-T
gnomAD v4: 1-165439867-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439867C>T , CM000663.2:g.165439867C>T GRCh38
NC_000001.10:g.165409104C>T , CM000663.1:g.165409104C>T GRCh37
NC_000001.9:g.163675728C>T NCBI36
NG_029517.1:g.10489G>A
NG_029517.2:g.10489G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+4978G>A MANE Select ENSP00000352900.5:n.49+4978G>A
ENST00000359842.9:c.49+4978G>A ENSP00000352900.5:n.49+4978G>A
ENST00000465764.1:n.329-2666G>A
ENST00000619224.1:c.-379+4978G>A ENSP00000482458.1:n.-379+4978G>A
NM_001256570.1:c.-379+4978G>A NP_001243499.1:n.-379+4978G>A
NM_006917.4:c.49+4978G>A NP_008848.1:n.49+4978G>A
NR_033824.1:n.512-2666G>A
NM_006917.5:c.49+4978G>A MANE Select NP_008848.1:n.49+4978G>A
NR_033824.2:n.283-2666G>A
NM_001256570.2:c.-379+4978G>A NP_001243499.1:n.-379+4978G>A
Search 100 bp 5'
Search 100 bp 3'