Canonical Allele Identifier: CA201058072
Gene: RXRA HGNC NCBI
COSMIC:
COSN14848035 (not active)
MyVariant.info:
GRCh38 chr9:g.134429009G>T
GRCh37 chr9:g.137320855G>T
gnomAD v2:
9:137320855 G / T
gnomAD v3:
9:134429009 G / T
gnomAD v4:
chr9-134429009-G-T
Joint Max Group AF 0.95938955 (AFR)
Genomes Max Group AF 0.95550436 (AFR)
Exomes Max Group AF 0.9588785 (AFR)
dbSNP:
3118570
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134429009G>T , CM000671.2:g.134429009G>T GRCh38
NC_000009.11:g.137320855G>T , CM000671.1:g.137320855G>T GRCh37
NC_000009.10:g.136460676G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.911-99G>T MANE Select ENSP00000419692.1:n.911-99G>T
ENST00000672570.1:c.830-99G>T ENSP00000500402.1:n.830-99G>T
ENST00000356384.4:n.1321-99G>T
ENST00000481739.1:c.911-99G>T ENSP00000419692.1:n.911-99G>T
NM_001291920.1:c.830-99G>T NP_001278849.1:n.830-99G>T
NM_001291921.1:c.620-99G>T NP_001278850.1:n.620-99G>T
NM_002957.5:c.911-99G>T NP_002948.1:n.911-99G>T
NM_002957.6:c.911-99G>T MANE Select NP_002948.1:n.911-99G>T
NM_001291921.2:c.620-99G>T NP_001278850.1:n.620-99G>T
NM_001291920.2:c.830-99G>T NP_001278849.1:n.830-99G>T
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