Canonical Allele Identifier: CA201049367
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs867468559

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375594G>A , CM000671.2:g.134375594G>A GRCh38
NC_000009.11:g.137267440G>A , CM000671.1:g.137267440G>A GRCh37
NC_000009.10:g.136407261G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-26038G>A MANE Select ENSP00000419692.1:n.29-26038G>A
ENST00000356384.4:n.293+1464G>A
ENST00000481739.1:c.29-26038G>A ENSP00000419692.1:n.29-26038G>A
ENST00000484822.1:n.453-26038G>A
NM_002957.5:c.29-26038G>A NP_002948.1:n.29-26038G>A
NM_002957.6:c.29-26038G>A MANE Select NP_002948.1:n.29-26038G>A