Canonical Allele Identifier: CA1883176721
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1831085088
gnomAD v4: 9-134408081-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408081A>G , CM000671.2:g.134408081A>G GRCh38
NC_000009.11:g.137299927A>G , CM000671.1:g.137299927A>G GRCh37
NC_000009.10:g.136439748A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.280-68A>G MANE Select ENSP00000419692.1:n.280-68A>G
ENST00000672570.1:c.199-68A>G ENSP00000500402.1:n.199-68A>G
ENST00000356384.4:n.690-68A>G
ENST00000481739.1:c.280-68A>G ENSP00000419692.1:n.280-68A>G
NM_001291920.1:c.199-68A>G NP_001278849.1:n.199-68A>G
NM_001291921.1:c.-12-68A>G NP_001278850.1:n.-12-68A>G
NM_002957.5:c.280-68A>G NP_002948.1:n.280-68A>G
NM_002957.6:c.280-68A>G MANE Select NP_002948.1:n.280-68A>G
NM_001291921.2:c.-12-68A>G NP_001278850.1:n.-12-68A>G
NM_001291920.2:c.199-68A>G NP_001278849.1:n.199-68A>G
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