Canonical Allele Identifier: CA2579504522
Gene: RXRA HGNC NCBI

Linked Data

gnomAD v4: 9-134408368-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408368T>A , CM000671.2:g.134408368T>A GRCh38
NC_000009.11:g.137300214T>A , CM000671.1:g.137300214T>A GRCh37
NC_000009.10:g.136440035T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.430+69T>A MANE Select ENSP00000419692.1:n.430+69T>A
ENST00000672570.1:c.349+69T>A ENSP00000500402.1:n.349+69T>A
ENST00000356384.4:n.840+69T>A
ENST00000481739.1:c.430+69T>A ENSP00000419692.1:n.430+69T>A
NM_001291920.1:c.349+69T>A NP_001278849.1:n.349+69T>A
NM_001291921.1:c.139+69T>A NP_001278850.1:n.139+69T>A
NM_002957.5:c.430+69T>A NP_002948.1:n.430+69T>A
NM_002957.6:c.430+69T>A MANE Select NP_002948.1:n.430+69T>A
NM_001291921.2:c.139+69T>A NP_001278850.1:n.139+69T>A
NM_001291920.2:c.349+69T>A NP_001278849.1:n.349+69T>A
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