Canonical Allele Identifier: CA1883155536
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375680C= , CM000671.2:g.134375680C= GRCh38
NC_000009.11:g.137267526C= , CM000671.1:g.137267526C= GRCh37
NC_000009.10:g.136407347C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-25952C= MANE Select ENSP00000419692.1:n.29-25952C=
ENST00000356384.4:n.293+1550C=
ENST00000481739.1:c.29-25952C= ENSP00000419692.1:n.29-25952C=
ENST00000484822.1:n.453-25952C=
NM_002957.5:c.29-25952C= NP_002948.1:n.29-25952C=
NM_002957.6:c.29-25952C= MANE Select NP_002948.1:n.29-25952C=
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