Canonical Allele Identifier: CA201084369

Gene: RXRA

Linked Data

• dbSNP Id: rs751064238
• gnomAD v2: 9-137300168-G-A
• gnomAD v4: 9-134408322-G-A
• MyVariant Identifiers: chr9:g.137300168G>A (hg19) ; chr9:g.134408322G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408322G>A , CM000671.2:g.134408322G>A	GRCh38
NC_000009.11:g.137300168G>A , CM000671.1:g.137300168G>A	GRCh37
NC_000009.10:g.136439989G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+23G>A MANE Select	ENSP00000419692.1:n.430+23G>A
ENST00000672570.1:c.349+23G>A	ENSP00000500402.1:n.349+23G>A
ENST00000356384.4:n.840+23G>A
ENST00000481739.1:c.430+23G>A	ENSP00000419692.1:n.430+23G>A
NM_001291920.1:c.349+23G>A	NP_001278849.1:n.349+23G>A
NM_001291921.1:c.139+23G>A	NP_001278850.1:n.139+23G>A
NM_002957.5:c.430+23G>A	NP_002948.1:n.430+23G>A
NM_002957.6:c.430+23G>A MANE Select	NP_002948.1:n.430+23G>A
NM_001291921.2:c.139+23G>A	NP_001278850.1:n.139+23G>A
NM_001291920.2:c.349+23G>A	NP_001278849.1:n.349+23G>A