Canonical Allele Identifier: CA467648581

Gene: RXRA

Linked Data

• dbSNP Id: rs766320897
• gnomAD v2: 9-137300051-C-T
• gnomAD v4: 9-134408205-C-T
• MyVariant Identifiers: chr9:g.137300051C>T (hg19) ; chr9:g.134408205C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408205C>T , CM000671.2:g.134408205C>T	GRCh38
NC_000009.11:g.137300051C>T , CM000671.1:g.137300051C>T	GRCh37
NC_000009.10:g.136439872C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.336C>T MANE Select	ENSP00000419692.1:p.Gly112=
ENST00000672570.1:c.255C>T	ENSP00000500402.1:p.Gly85=
ENST00000356384.4:n.746C>T
ENST00000481739.1:c.336C>T	ENSP00000419692.1:p.Gly112=
NM_001291920.1:c.255C>T	NP_001278849.1:p.Gly85=
NM_001291921.1:c.45C>T	NP_001278850.1:p.Gly15=
NM_002957.5:c.336C>T	NP_002948.1:p.Gly112=
NM_002957.6:c.336C>T MANE Select	NP_002948.1:p.Gly112=
NM_001291921.2:c.45C>T	NP_001278850.1:p.Gly15=
NM_001291920.2:c.255C>T	NP_001278849.1:p.Gly85=