Canonical Allele Identifier: CA591092941
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1326882749
gnomAD v2: 9-137267408-C-T
gnomAD v3: 9-134375562-C-T
gnomAD v4: 9-134375562-C-T
MyVariant Identifiers: chr9:g.137267408C>T (hg19) chr9:g.134375562C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375562C>T , CM000671.2:g.134375562C>T GRCh38
NC_000009.11:g.137267408C>T , CM000671.1:g.137267408C>T GRCh37
NC_000009.10:g.136407229C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-26070C>T MANE Select ENSP00000419692.1:n.29-26070C>T
ENST00000356384.4:n.293+1432C>T
ENST00000481739.1:c.29-26070C>T ENSP00000419692.1:n.29-26070C>T
ENST00000484822.1:n.453-26070C>T
NM_002957.5:c.29-26070C>T NP_002948.1:n.29-26070C>T
NM_002957.6:c.29-26070C>T MANE Select NP_002948.1:n.29-26070C>T
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