Canonical Allele Identifier: CA467649059

Gene: RXRA

Linked Data

• dbSNP Id: rs1269539322
• gnomAD v2: 9-137300138-C-T
• gnomAD v4: 9-134408292-C-T
• MyVariant Identifiers: chr9:g.137300138C>T (hg19) ; chr9:g.134408292C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408292C>T , CM000671.2:g.134408292C>T	GRCh38
NC_000009.11:g.137300138C>T , CM000671.1:g.137300138C>T	GRCh37
NC_000009.10:g.136439959C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.423C>T MANE Select	ENSP00000419692.1:p.Arg141=
ENST00000672570.1:c.342C>T	ENSP00000500402.1:p.Arg114=
ENST00000356384.4:n.833C>T
ENST00000481739.1:c.423C>T	ENSP00000419692.1:p.Arg141=
NM_001291920.1:c.342C>T	NP_001278849.1:p.Arg114=
NM_001291921.1:c.132C>T	NP_001278850.1:p.Arg44=
NM_002957.5:c.423C>T	NP_002948.1:p.Arg141=
NM_002957.6:c.423C>T MANE Select	NP_002948.1:p.Arg141=
NM_001291921.2:c.132C>T	NP_001278850.1:p.Arg44=
NM_001291920.2:c.342C>T	NP_001278849.1:p.Arg114=