Canonical Allele Identifier: CA1883155518
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1830546722

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134375646G>C , CM000671.2:g.134375646G>C GRCh38
NC_000009.11:g.137267492G>C , CM000671.1:g.137267492G>C GRCh37
NC_000009.10:g.136407313G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.29-25986G>C MANE Select ENSP00000419692.1:n.29-25986G>C
ENST00000356384.4:n.293+1516G>C
ENST00000481739.1:c.29-25986G>C ENSP00000419692.1:n.29-25986G>C
ENST00000484822.1:n.453-25986G>C
NM_002957.5:c.29-25986G>C NP_002948.1:n.29-25986G>C
NM_002957.6:c.29-25986G>C MANE Select NP_002948.1:n.29-25986G>C