Canonical Allele Identifier: CA201041275
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs773420230
gnomAD v2: 9-137301752-G-A
gnomAD v3: 9-134409906-G-A
gnomAD v4: 9-134409906-G-A
MyVariant Identifiers: chr9:g.137301752G>A (hg19) chr9:g.134409906G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409906G>A , CM000671.2:g.134409906G>A GRCh38
NC_000009.11:g.137301752G>A , CM000671.1:g.137301752G>A GRCh37
NC_000009.10:g.136441573G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.610+787G>A MANE Select ENSP00000419692.1:n.610+787G>A
ENST00000672570.1:c.529+787G>A ENSP00000500402.1:n.529+787G>A
ENST00000356384.4:n.1020+787G>A
ENST00000481739.1:c.610+787G>A ENSP00000419692.1:n.610+787G>A
NM_001291920.1:c.529+787G>A NP_001278849.1:n.529+787G>A
NM_001291921.1:c.319+787G>A NP_001278850.1:n.319+787G>A
NM_002957.5:c.610+787G>A NP_002948.1:n.610+787G>A
NM_002957.6:c.610+787G>A MANE Select NP_002948.1:n.610+787G>A
NM_001291921.2:c.319+787G>A NP_001278850.1:n.319+787G>A
NM_001291920.2:c.529+787G>A NP_001278849.1:n.529+787G>A
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