Canonical Allele Identifier: CA467648481

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408187-C-T
• MyVariant Identifiers: chr9:g.137300033C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408187C>T , CM000671.2:g.134408187C>T	GRCh38
NC_000009.11:g.137300033C>T , CM000671.1:g.137300033C>T	GRCh37
NC_000009.10:g.136439854C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.318C>T MANE Select	ENSP00000419692.1:p.Asp106=
ENST00000672570.1:c.237C>T	ENSP00000500402.1:p.Asp79=
ENST00000356384.4:n.728C>T
ENST00000481739.1:c.318C>T	ENSP00000419692.1:p.Asp106=
NM_001291920.1:c.237C>T	NP_001278849.1:p.Asp79=
NM_001291921.1:c.27C>T	NP_001278850.1:p.Asp9=
NM_002957.5:c.318C>T	NP_002948.1:p.Asp106=
NM_002957.6:c.318C>T MANE Select	NP_002948.1:p.Asp106=
NM_001291921.2:c.27C>T	NP_001278850.1:p.Asp9=
NM_001291920.2:c.237C>T	NP_001278849.1:p.Asp79=