Canonical Allele Identifier: CA467647880

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408175-C-T
• MyVariant Identifiers: chr9:g.137300021C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408175C>T , CM000671.2:g.134408175C>T	GRCh38
NC_000009.11:g.137300021C>T , CM000671.1:g.137300021C>T	GRCh37
NC_000009.10:g.136439842C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.306C>T MANE Select	ENSP00000419692.1:p.Ser102=
ENST00000672570.1:c.225C>T	ENSP00000500402.1:p.Ser75=
ENST00000356384.4:n.716C>T
ENST00000481739.1:c.306C>T	ENSP00000419692.1:p.Ser102=
NM_001291920.1:c.225C>T	NP_001278849.1:p.Ser75=
NM_001291921.1:c.15C>T	NP_001278850.1:p.Ser5=
NM_002957.5:c.306C>T	NP_002948.1:p.Ser102=
NM_002957.6:c.306C>T MANE Select	NP_002948.1:p.Ser102=
NM_001291921.2:c.15C>T	NP_001278850.1:p.Ser5=
NM_001291920.2:c.225C>T	NP_001278849.1:p.Ser75=