Canonical Allele Identifier: CA1883155464
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375547T= , CM000671.2:g.134375547T= GRCh38
NC_000009.11:g.137267393T= , CM000671.1:g.137267393T= GRCh37
NC_000009.10:g.136407214T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-26085T= MANE Select ENSP00000419692.1:n.29-26085T=
ENST00000356384.4:n.293+1417T=
ENST00000481739.1:c.29-26085T= ENSP00000419692.1:n.29-26085T=
ENST00000484822.1:n.453-26085T=
NM_002957.5:c.29-26085T= NP_002948.1:n.29-26085T=
NM_002957.6:c.29-26085T= MANE Select NP_002948.1:n.29-26085T=