Canonical Allele Identifier: CA860857752

Gene: RXRA

Linked Data

• dbSNP Id: rs1470977177
• gnomAD v3: 9-134409823-T-C
• gnomAD v4: 9-134409823-T-C
• MyVariant Identifiers: chr9:g.137301669T>C (hg19) ; chr9:g.134409823T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134409823T>C , CM000671.2:g.134409823T>C	GRCh38
NC_000009.11:g.137301669T>C , CM000671.1:g.137301669T>C	GRCh37
NC_000009.10:g.136441490T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.610+704T>C MANE Select	ENSP00000419692.1:n.610+704T>C
ENST00000672570.1:c.529+704T>C	ENSP00000500402.1:n.529+704T>C
ENST00000356384.4:n.1020+704T>C
ENST00000481739.1:c.610+704T>C	ENSP00000419692.1:n.610+704T>C
NM_001291920.1:c.529+704T>C	NP_001278849.1:n.529+704T>C
NM_001291921.1:c.319+704T>C	NP_001278850.1:n.319+704T>C
NM_002957.5:c.610+704T>C	NP_002948.1:n.610+704T>C
NM_002957.6:c.610+704T>C MANE Select	NP_002948.1:n.610+704T>C
NM_001291921.2:c.319+704T>C	NP_001278850.1:n.319+704T>C
NM_001291920.2:c.529+704T>C	NP_001278849.1:n.529+704T>C