Canonical Allele Identifier: CA1883155492
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375596C= , CM000671.2:g.134375596C= GRCh38
NC_000009.11:g.137267442C= , CM000671.1:g.137267442C= GRCh37
NC_000009.10:g.136407263C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-26036C= MANE Select ENSP00000419692.1:n.29-26036C=
ENST00000356384.4:n.293+1466C=
ENST00000481739.1:c.29-26036C= ENSP00000419692.1:n.29-26036C=
ENST00000484822.1:n.453-26036C=
NM_002957.5:c.29-26036C= NP_002948.1:n.29-26036C=
NM_002957.6:c.29-26036C= MANE Select NP_002948.1:n.29-26036C=