Canonical Allele Identifier: CA1883155421
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375473A= , CM000671.2:g.134375473A= GRCh38
NC_000009.11:g.137267319A= , CM000671.1:g.137267319A= GRCh37
NC_000009.10:g.136407140A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-26159A= MANE Select ENSP00000419692.1:n.29-26159A=
ENST00000356384.4:n.293+1343A=
ENST00000481739.1:c.29-26159A= ENSP00000419692.1:n.29-26159A=
ENST00000484822.1:n.453-26159A=
NM_002957.5:c.29-26159A= NP_002948.1:n.29-26159A=
NM_002957.6:c.29-26159A= MANE Select NP_002948.1:n.29-26159A=
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