Canonical Allele Identifier: CA201041176

Gene: RXRA

Linked Data

• dbSNP Id: rs568147587
• gnomAD v3: 9-134409763-G-C
• gnomAD v4: 9-134409763-G-C
• MyVariant Identifiers: chr9:g.137301609G>C (hg19) ; chr9:g.134409763G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134409763G>C , CM000671.2:g.134409763G>C	GRCh38
NC_000009.11:g.137301609G>C , CM000671.1:g.137301609G>C	GRCh37
NC_000009.10:g.136441430G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.610+644G>C MANE Select	ENSP00000419692.1:n.610+644G>C
ENST00000672570.1:c.529+644G>C	ENSP00000500402.1:n.529+644G>C
ENST00000356384.4:n.1020+644G>C
ENST00000481739.1:c.610+644G>C	ENSP00000419692.1:n.610+644G>C
NM_001291920.1:c.529+644G>C	NP_001278849.1:n.529+644G>C
NM_001291921.1:c.319+644G>C	NP_001278850.1:n.319+644G>C
NM_002957.5:c.610+644G>C	NP_002948.1:n.610+644G>C
NM_002957.6:c.610+644G>C MANE Select	NP_002948.1:n.610+644G>C
NM_001291921.2:c.319+644G>C	NP_001278850.1:n.319+644G>C
NM_001291920.2:c.529+644G>C	NP_001278849.1:n.529+644G>C