Canonical Allele Identifier: CA13003117
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs7864987
gnomAD v2: 9-137248166-T-C
gnomAD v3: 9-134356320-T-C
gnomAD v4: 9-134356320-T-C
MyVariant Identifiers: chr9:g.137248166T>C (hg19) chr9:g.137248166_137248167delinsCG (hg19) chr9:g.134356320T>C (hg38) chr9:g.134356320_134356321delinsCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134356320T>C , CM000671.2:g.134356320T>C GRCh38
NC_000009.11:g.137248166T>C , CM000671.1:g.137248166T>C GRCh37
NC_000009.10:g.136387987T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.28+29661T>C MANE Select ENSP00000419692.1:n.28+29661T>C
ENST00000481739.1:c.28+29661T>C ENSP00000419692.1:n.28+29661T>C
ENST00000484822.1:n.452+36836T>C
NM_002957.5:c.28+29661T>C NP_002948.1:n.28+29661T>C
NM_002957.6:c.28+29661T>C MANE Select NP_002948.1:n.28+29661T>C
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