Canonical Allele Identifier: CA890557540
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs1449674236
gnomAD v3: 1-165439911-G-C
gnomAD v4: 1-165439911-G-C
MyVariant Identifiers: chr1:g.165409148G>C (hg19) chr1:g.165439911G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165439911G>C , CM000663.2:g.165439911G>C GRCh38
NC_000001.10:g.165409148G>C , CM000663.1:g.165409148G>C GRCh37
NC_000001.9:g.163675772G>C NCBI36
NG_029517.1:g.10445C>G
NG_029517.2:g.10445C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.49+4934C>G MANE Select ENSP00000352900.5:n.49+4934C>G
ENST00000359842.9:c.49+4934C>G ENSP00000352900.5:n.49+4934C>G
ENST00000465764.1:n.329-2710C>G
ENST00000619224.1:c.-379+4934C>G ENSP00000482458.1:n.-379+4934C>G
NM_001256570.1:c.-379+4934C>G NP_001243499.1:n.-379+4934C>G
NM_006917.4:c.49+4934C>G NP_008848.1:n.49+4934C>G
NR_033824.1:n.512-2710C>G
NM_006917.5:c.49+4934C>G MANE Select NP_008848.1:n.49+4934C>G
NR_033824.2:n.283-2710C>G
NM_001256570.2:c.-379+4934C>G NP_001243499.1:n.-379+4934C>G
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