Canonical Allele Identifier: CA201049431

Gene: RXRA

Linked Data

• dbSNP Id: rs934752364
• gnomAD v2: 9-137267467-C-T
• gnomAD v3: 9-134375621-C-T
• gnomAD v4: 9-134375621-C-T
• MyVariant Identifiers: chr9:g.137267467C>T (hg19) ; chr9:g.134375621C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134375621C>T , CM000671.2:g.134375621C>T	GRCh38
NC_000009.11:g.137267467C>T , CM000671.1:g.137267467C>T	GRCh37
NC_000009.10:g.136407288C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.29-26011C>T MANE Select	ENSP00000419692.1:n.29-26011C>T
ENST00000356384.4:n.293+1491C>T
ENST00000481739.1:c.29-26011C>T	ENSP00000419692.1:n.29-26011C>T
ENST00000484822.1:n.453-26011C>T
NM_002957.5:c.29-26011C>T	NP_002948.1:n.29-26011C>T
NM_002957.6:c.29-26011C>T MANE Select	NP_002948.1:n.29-26011C>T