Canonical Allele Identifier: CA860872610

Gene: RXRA

Linked Data

• dbSNP Id: rs1414054888
• gnomAD v3: 9-134432132-C-T
• gnomAD v4: 9-134432132-C-T
• MyVariant Identifiers: chr9:g.137323978C>T (hg19) ; chr9:g.134432132C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134432132C>T , CM000671.2:g.134432132C>T	GRCh38
NC_000009.11:g.137323978C>T , CM000671.1:g.137323978C>T	GRCh37
NC_000009.10:g.136463799C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.1135+136C>T MANE Select	ENSP00000419692.1:n.1135+136C>T
ENST00000672570.1:c.1054+136C>T	ENSP00000500402.1:n.1054+136C>T
ENST00000356384.4:n.1545+136C>T
ENST00000481739.1:c.1135+136C>T	ENSP00000419692.1:n.1135+136C>T
NM_001291920.1:c.1054+136C>T	NP_001278849.1:n.1054+136C>T
NM_001291921.1:c.844+136C>T	NP_001278850.1:n.844+136C>T
NM_002957.5:c.1135+136C>T	NP_002948.1:n.1135+136C>T
NM_002957.6:c.1135+136C>T MANE Select	NP_002948.1:n.1135+136C>T
NM_001291921.2:c.844+136C>T	NP_001278850.1:n.844+136C>T
NM_001291920.2:c.1054+136C>T	NP_001278849.1:n.1054+136C>T