Canonical Allele Identifier: CA2692438848
Gene: RXRA HGNC NCBI

Linked Data

gnomAD v4: 9-134432118-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134432118G>T , CM000671.2:g.134432118G>T GRCh38
NC_000009.11:g.137323964G>T , CM000671.1:g.137323964G>T GRCh37
NC_000009.10:g.136463785G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.1135+122G>T MANE Select ENSP00000419692.1:n.1135+122G>T
ENST00000672570.1:c.1054+122G>T ENSP00000500402.1:n.1054+122G>T
ENST00000356384.4:n.1545+122G>T
ENST00000481739.1:c.1135+122G>T ENSP00000419692.1:n.1135+122G>T
NM_001291920.1:c.1054+122G>T NP_001278849.1:n.1054+122G>T
NM_001291921.1:c.844+122G>T NP_001278850.1:n.844+122G>T
NM_002957.5:c.1135+122G>T NP_002948.1:n.1135+122G>T
NM_002957.6:c.1135+122G>T MANE Select NP_002948.1:n.1135+122G>T
NM_001291921.2:c.844+122G>T NP_001278850.1:n.844+122G>T
NM_001291920.2:c.1054+122G>T NP_001278849.1:n.1054+122G>T
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