Canonical Allele Identifier: CA2786203399
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375692T>A , CM000671.2:g.134375692T>A GRCh38
NC_000009.11:g.137267538T>A , CM000671.1:g.137267538T>A GRCh37
NC_000009.10:g.136407359T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-25940T>A MANE Select ENSP00000419692.1:n.29-25940T>A
ENST00000356384.4:n.293+1562T>A
ENST00000481739.1:c.29-25940T>A ENSP00000419692.1:n.29-25940T>A
ENST00000484822.1:n.453-25940T>A
NM_002957.5:c.29-25940T>A NP_002948.1:n.29-25940T>A
NM_002957.6:c.29-25940T>A MANE Select NP_002948.1:n.29-25940T>A