Canonical Allele Identifier: CA15080615
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs2651860
gnomAD v2: 1-165381055-A-C
gnomAD v3: 1-165411818-A-C
gnomAD v4: 1-165411818-A-C
MyVariant Identifiers: chr1:g.165381055A>C (hg19) chr1:g.165411818A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165411818A>C , CM000663.2:g.165411818A>C GRCh38
NC_000001.10:g.165381055A>C , CM000663.1:g.165381055A>C GRCh37
NC_000001.9:g.163647679A>C NCBI36
NG_029517.1:g.38538T>G
NG_029517.2:g.38538T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.623-709T>G MANE Select ENSP00000352900.5:n.623-709T>G
ENST00000359842.9:c.623-709T>G ENSP00000352900.5:n.623-709T>G
ENST00000470566.1:n.548-709T>G
ENST00000619224.1:c.254-709T>G ENSP00000482458.1:n.254-709T>G
NM_001256570.1:c.254-709T>G NP_001243499.1:n.254-709T>G
NM_001256571.1:c.254-709T>G NP_001243500.1:n.254-709T>G
NM_006917.4:c.623-709T>G NP_008848.1:n.623-709T>G
NM_006917.5:c.623-709T>G MANE Select NP_008848.1:n.623-709T>G
NM_001256571.2:c.254-709T>G NP_001243500.1:n.254-709T>G
NM_001256570.2:c.254-709T>G NP_001243499.1:n.254-709T>G
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