Canonical Allele Identifier: CA860857861
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1327086197
MyVariant Identifiers: chr9:g.137301818T>C (hg19) chr9:g.134409972T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409972T>C , CM000671.2:g.134409972T>C GRCh38
NC_000009.11:g.137301818T>C , CM000671.1:g.137301818T>C GRCh37
NC_000009.10:g.136441639T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.610+853T>C MANE Select ENSP00000419692.1:n.610+853T>C
ENST00000672570.1:c.529+853T>C ENSP00000500402.1:n.529+853T>C
ENST00000356384.4:n.1020+853T>C
ENST00000481739.1:c.610+853T>C ENSP00000419692.1:n.610+853T>C
NM_001291920.1:c.529+853T>C NP_001278849.1:n.529+853T>C
NM_001291921.1:c.319+853T>C NP_001278850.1:n.319+853T>C
NM_002957.5:c.610+853T>C NP_002948.1:n.610+853T>C
NM_002957.6:c.610+853T>C MANE Select NP_002948.1:n.610+853T>C
NM_001291921.2:c.319+853T>C NP_001278850.1:n.319+853T>C
NM_001291920.2:c.529+853T>C NP_001278849.1:n.529+853T>C
Search 100 bp 5'
Search 100 bp 3'