Canonical Allele Identifier: CA375451996
Gene: RXRA HGNC NCBI

Linked Data

gnomAD v4: 9-134408162-T-C
MyVariant Identifiers: chr9:g.137300008T>C (hg19) chr9:g.134408162T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408162T>C , CM000671.2:g.134408162T>C GRCh38
NC_000009.11:g.137300008T>C , CM000671.1:g.137300008T>C GRCh37
NC_000009.10:g.136439829T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.293T>C MANE Select ENSP00000419692.1:p.Met98Thr
ENST00000672570.1:c.212T>C ENSP00000500402.1:p.Met71Thr
ENST00000356384.4:n.703T>C
ENST00000481739.1:c.293T>C ENSP00000419692.1:p.Met98Thr
NM_001291920.1:c.212T>C NP_001278849.1:p.Met71Thr
NM_001291921.1:c.2T>C NP_001278850.1:p.Met1Thr
NM_002957.5:c.293T>C NP_002948.1:p.Met98Thr
NM_002957.6:c.293T>C MANE Select NP_002948.1:p.Met98Thr
NM_001291921.2:c.2T>C NP_001278850.1:p.Met1Thr
NM_001291920.2:c.212T>C NP_001278849.1:p.Met71Thr
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