Canonical Allele Identifier: CA1883147333
Gene: RXRA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134356220G= , CM000671.2:g.134356220G= GRCh38
NC_000009.11:g.137248066G= , CM000671.1:g.137248066G= GRCh37
NC_000009.10:g.136387887G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.28+29561G= MANE Select ENSP00000419692.1:n.28+29561G=
ENST00000481739.1:c.28+29561G= ENSP00000419692.1:n.28+29561G=
ENST00000484822.1:n.452+36736G=
NM_002957.5:c.28+29561G= NP_002948.1:n.28+29561G=
NM_002957.6:c.28+29561G= MANE Select NP_002948.1:n.28+29561G=
Search 100 bp 5'
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