Canonical Allele Identifier: CA375451910
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137299996T>G (hg19) chr9:g.134408150T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408150T>G , CM000671.2:g.134408150T>G GRCh38
NC_000009.11:g.137299996T>G , CM000671.1:g.137299996T>G GRCh37
NC_000009.10:g.136439817T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.281T>G MANE Select ENSP00000419692.1:p.Leu94Arg
ENST00000672570.1:c.200T>G ENSP00000500402.1:p.Leu67Arg
ENST00000356384.4:n.691T>G
ENST00000481739.1:c.281T>G ENSP00000419692.1:p.Leu94Arg
NM_001291920.1:c.200T>G NP_001278849.1:p.Leu67Arg
NM_001291921.1:c.-11T>G NP_001278850.1:n.-11T>G
NM_002957.5:c.281T>G NP_002948.1:p.Leu94Arg
NM_002957.6:c.281T>G MANE Select NP_002948.1:p.Leu94Arg
NM_001291921.2:c.-11T>G NP_001278850.1:n.-11T>G
NM_001291920.2:c.200T>G NP_001278849.1:p.Leu67Arg
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