Canonical Allele Identifier: CA375452327
Gene: RXRA HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137300069G>C (hg19) chr9:g.134408223G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408223G>C , CM000671.2:g.134408223G>C GRCh38
NC_000009.11:g.137300069G>C , CM000671.1:g.137300069G>C GRCh37
NC_000009.10:g.136439890G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.354G>C MANE Select ENSP00000419692.1:p.Lys118Asn
ENST00000672570.1:c.273G>C ENSP00000500402.1:p.Lys91Asn
ENST00000356384.4:n.764G>C
ENST00000481739.1:c.354G>C ENSP00000419692.1:p.Lys118Asn
NM_001291920.1:c.273G>C NP_001278849.1:p.Lys91Asn
NM_001291921.1:c.63G>C NP_001278850.1:p.Lys21Asn
NM_002957.5:c.354G>C NP_002948.1:p.Lys118Asn
NM_002957.6:c.354G>C MANE Select NP_002948.1:p.Lys118Asn
NM_001291921.2:c.63G>C NP_001278850.1:p.Lys21Asn
NM_001291920.2:c.273G>C NP_001278849.1:p.Lys91Asn
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