Canonical Allele Identifier: CA5317722
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs201880753
ExAC: 9:137300095 T / C
gnomAD v2: 9-137300095-T-C
gnomAD v3: 9-134408249-T-C
gnomAD v4: 9-134408249-T-C
MyVariant Identifiers: chr9:g.137300095T>C (hg19) chr9:g.134408249T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408249T>C , CM000671.2:g.134408249T>C GRCh38
NC_000009.11:g.137300095T>C , CM000671.1:g.137300095T>C GRCh37
NC_000009.10:g.136439916T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.380T>C MANE Select ENSP00000419692.1:p.Met127Thr
ENST00000672570.1:c.299T>C ENSP00000500402.1:p.Met100Thr
ENST00000356384.4:n.790T>C
ENST00000481739.1:c.380T>C ENSP00000419692.1:p.Met127Thr
NM_001291920.1:c.299T>C NP_001278849.1:p.Met100Thr
NM_001291921.1:c.89T>C NP_001278850.1:p.Met30Thr
NM_002957.5:c.380T>C NP_002948.1:p.Met127Thr
NM_002957.6:c.380T>C MANE Select NP_002948.1:p.Met127Thr
NM_001291921.2:c.89T>C NP_001278850.1:p.Met30Thr
NM_001291920.2:c.299T>C NP_001278849.1:p.Met100Thr
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