Canonical Allele Identifier: CA1883155531
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375672C= , CM000671.2:g.134375672C= GRCh38
NC_000009.11:g.137267518C= , CM000671.1:g.137267518C= GRCh37
NC_000009.10:g.136407339C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-25960C= MANE Select ENSP00000419692.1:n.29-25960C=
ENST00000356384.4:n.293+1542C=
ENST00000481739.1:c.29-25960C= ENSP00000419692.1:n.29-25960C=
ENST00000484822.1:n.453-25960C=
NM_002957.5:c.29-25960C= NP_002948.1:n.29-25960C=
NM_002957.6:c.29-25960C= MANE Select NP_002948.1:n.29-25960C=
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