Canonical Allele Identifier: CA890557501
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs1290412149
gnomAD v3: 1-165439796-AAC-A
gnomAD v4: 1-165439796-AAC-A
MyVariant Identifiers: chr1:g.165409034_165409035del (hg19) chr1:g.165439797_165439798del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439798_165439799del , CM000663.2:g.165439798_165439799del GRCh38
NC_000001.10:g.165409035_165409036del , CM000663.1:g.165409035_165409036del GRCh37
NC_000001.9:g.163675659_163675660del NCBI36
NG_029517.1:g.10558_10559del
NG_029517.2:g.10558_10559del

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+5047_49+5048del MANE Select ENSP00000352900.5:n.49+5047_49+5048del
ENST00000359842.9:c.49+5047_49+5048del ENSP00000352900.5:n.49+5047_49+5048del
ENST00000465764.1:n.329-2597_329-2596del
ENST00000619224.1:c.-379+5047_-379+5048del ENSP00000482458.1:n.-379+5047_-379+5048de...
NM_001256570.1:c.-379+5047_-379+5048del NP_001243499.1:n.-379+5047_-379+5048del
NM_006917.4:c.49+5047_49+5048del NP_008848.1:n.49+5047_49+5048del
NR_033824.1:n.512-2597_512-2596del
NM_006917.5:c.49+5047_49+5048del MANE Select NP_008848.1:n.49+5047_49+5048del
NR_033824.2:n.283-2597_283-2596del
NM_001256570.2:c.-379+5047_-379+5048del NP_001243499.1:n.-379+5047_-379+5048del
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