Canonical Allele Identifier: CA2692438857
Gene: RXRA HGNC NCBI

Linked Data

gnomAD v4: 9-134432122-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134432122T>G , CM000671.2:g.134432122T>G GRCh38
NC_000009.11:g.137323968T>G , CM000671.1:g.137323968T>G GRCh37
NC_000009.10:g.136463789T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.1135+126T>G MANE Select ENSP00000419692.1:n.1135+126T>G
ENST00000672570.1:c.1054+126T>G ENSP00000500402.1:n.1054+126T>G
ENST00000356384.4:n.1545+126T>G
ENST00000481739.1:c.1135+126T>G ENSP00000419692.1:n.1135+126T>G
NM_001291920.1:c.1054+126T>G NP_001278849.1:n.1054+126T>G
NM_001291921.1:c.844+126T>G NP_001278850.1:n.844+126T>G
NM_002957.5:c.1135+126T>G NP_002948.1:n.1135+126T>G
NM_002957.6:c.1135+126T>G MANE Select NP_002948.1:n.1135+126T>G
NM_001291921.2:c.844+126T>G NP_001278850.1:n.844+126T>G
NM_001291920.2:c.1054+126T>G NP_001278849.1:n.1054+126T>G
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