Canonical Allele Identifier: CA201041300

Gene: RXRA

Linked Data

• dbSNP Id: rs900636454
• gnomAD v2: 9-137301802-G-A
• gnomAD v3: 9-134409956-G-A
• gnomAD v4: 9-134409956-G-A
• MyVariant Identifiers: chr9:g.137301802G>A (hg19) ; chr9:g.134409956G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134409956G>A , CM000671.2:g.134409956G>A	GRCh38
NC_000009.11:g.137301802G>A , CM000671.1:g.137301802G>A	GRCh37
NC_000009.10:g.136441623G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.610+837G>A MANE Select	ENSP00000419692.1:n.610+837G>A
ENST00000672570.1:c.529+837G>A	ENSP00000500402.1:n.529+837G>A
ENST00000356384.4:n.1020+837G>A
ENST00000481739.1:c.610+837G>A	ENSP00000419692.1:n.610+837G>A
NM_001291920.1:c.529+837G>A	NP_001278849.1:n.529+837G>A
NM_001291921.1:c.319+837G>A	NP_001278850.1:n.319+837G>A
NM_002957.5:c.610+837G>A	NP_002948.1:n.610+837G>A
NM_002957.6:c.610+837G>A MANE Select	NP_002948.1:n.610+837G>A
NM_001291921.2:c.319+837G>A	NP_001278850.1:n.319+837G>A
NM_001291920.2:c.529+837G>A	NP_001278849.1:n.529+837G>A