Canonical Allele Identifier: CA2720599807
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs2119089912

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375551_134375552del , CM000671.2:g.134375551_134375552del GRCh38
NC_000009.11:g.137267397_137267398del , CM000671.1:g.137267397_137267398del GRCh37
NC_000009.10:g.136407218_136407219del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-26081_29-26080del MANE Select ENSP00000419692.1:n.29-26081_29-26080del
ENST00000356384.4:n.293+1421_293+1422del
ENST00000481739.1:c.29-26081_29-26080del ENSP00000419692.1:n.29-26081_29-26080del
ENST00000484822.1:n.453-26081_453-26080del
NM_002957.5:c.29-26081_29-26080del NP_002948.1:n.29-26081_29-26080del
NM_002957.6:c.29-26081_29-26080del MANE Select NP_002948.1:n.29-26081_29-26080del