Canonical Allele Identifier: CA1883147345
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134356244C= , CM000671.2:g.134356244C= GRCh38
NC_000009.11:g.137248090C= , CM000671.1:g.137248090C= GRCh37
NC_000009.10:g.136387911C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.28+29585C= MANE Select ENSP00000419692.1:n.28+29585C=
ENST00000481739.1:c.28+29585C= ENSP00000419692.1:n.28+29585C=
ENST00000484822.1:n.452+36760C=
NM_002957.5:c.28+29585C= NP_002948.1:n.28+29585C=
NM_002957.6:c.28+29585C= MANE Select NP_002948.1:n.28+29585C=