Canonical Allele Identifier: CA860853281

Gene: RXRA

Linked Data

• dbSNP Id: rs1280772334
• gnomAD v3: 9-134398781-G-C
• gnomAD v4: 9-134398781-G-C
• MyVariant Identifiers: chr9:g.137290627G>C (hg19) ; chr9:g.134398781G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134398781G>C , CM000671.2:g.134398781G>C	GRCh38
NC_000009.11:g.137290627G>C , CM000671.1:g.137290627G>C	GRCh37
NC_000009.10:g.136430448G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.29-2851G>C MANE Select	ENSP00000419692.1:n.29-2851G>C
ENST00000649020.1:c.119-2851G>C	ENSP00000497073.1:n.119-2851G>C
ENST00000672570.1:c.-53-2851G>C	ENSP00000500402.1:n.-53-2851G>C
ENST00000356384.4:n.294-2615G>C
ENST00000481739.1:c.29-2851G>C	ENSP00000419692.1:n.29-2851G>C
ENST00000484822.1:n.453-2851G>C
NM_001291920.1:c.-53-2851G>C	NP_001278849.1:n.-53-2851G>C
NM_002957.5:c.29-2851G>C	NP_002948.1:n.29-2851G>C
NM_002957.6:c.29-2851G>C MANE Select	NP_002948.1:n.29-2851G>C
NM_001291920.2:c.-53-2851G>C	NP_001278849.1:n.-53-2851G>C