Canonical Allele Identifier: CA12974929
Gene: RXRA HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.134433976T>C
GRCh37 chr9:g.137325822T>C
gnomAD v2:
9:137325822 T / C
gnomAD v3:
9:134433976 T / C
gnomAD v4:
chr9-134433976-T-C
Joint Max Group AF 0.94207859 (AFR)
Genomes Max Group AF 0.94082408 (AFR)
Exomes Max Group AF 0.93586631 (AFR)
dbSNP:
3132293
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134433976T>C , CM000671.2:g.134433976T>C GRCh38
NC_000009.11:g.137325822T>C , CM000671.1:g.137325822T>C GRCh37
NC_000009.10:g.136465643T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.1136-126T>C MANE Select ENSP00000419692.1:n.1136-126T>C
ENST00000672570.1:c.1055-126T>C ENSP00000500402.1:n.1055-126T>C
ENST00000356384.4:n.1546-126T>C
ENST00000481739.1:c.1136-126T>C ENSP00000419692.1:n.1136-126T>C
NM_001291920.1:c.1055-126T>C NP_001278849.1:n.1055-126T>C
NM_001291921.1:c.845-126T>C NP_001278850.1:n.845-126T>C
NM_002957.5:c.1136-126T>C NP_002948.1:n.1136-126T>C
NM_002957.6:c.1136-126T>C MANE Select NP_002948.1:n.1136-126T>C
NM_001291921.2:c.845-126T>C NP_001278850.1:n.845-126T>C
NM_001291920.2:c.1055-126T>C NP_001278849.1:n.1055-126T>C
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