Canonical Allele Identifier: CA375452467
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137300092A>C (hg19) chr9:g.134408246A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408246A>C , CM000671.2:g.134408246A>C GRCh38
NC_000009.11:g.137300092A>C , CM000671.1:g.137300092A>C GRCh37
NC_000009.10:g.136439913A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.377A>C MANE Select ENSP00000419692.1:p.Asn126Thr
ENST00000672570.1:c.296A>C ENSP00000500402.1:p.Asn99Thr
ENST00000356384.4:n.787A>C
ENST00000481739.1:c.377A>C ENSP00000419692.1:p.Asn126Thr
NM_001291920.1:c.296A>C NP_001278849.1:p.Asn99Thr
NM_001291921.1:c.86A>C NP_001278850.1:p.Asn29Thr
NM_002957.5:c.377A>C NP_002948.1:p.Asn126Thr
NM_002957.6:c.377A>C MANE Select NP_002948.1:p.Asn126Thr
NM_001291921.2:c.86A>C NP_001278850.1:p.Asn29Thr
NM_001291920.2:c.296A>C NP_001278849.1:p.Asn99Thr
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