Canonical Allele Identifier: CA1883155429
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375484G= , CM000671.2:g.134375484G= GRCh38
NC_000009.11:g.137267330G= , CM000671.1:g.137267330G= GRCh37
NC_000009.10:g.136407151G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-26148G= MANE Select ENSP00000419692.1:n.29-26148G=
ENST00000356384.4:n.293+1354G=
ENST00000481739.1:c.29-26148G= ENSP00000419692.1:n.29-26148G=
ENST00000484822.1:n.453-26148G=
NM_002957.5:c.29-26148G= NP_002948.1:n.29-26148G=
NM_002957.6:c.29-26148G= MANE Select NP_002948.1:n.29-26148G=