Canonical Allele Identifier: CA5317698

Gene: RXRA

Linked Data

• dbSNP Id: rs778453074
• ExAC: 9:137300002 C / T
• gnomAD v2: 9-137300002-C-T
• gnomAD v4: 9-134408156-C-T
• MyVariant Identifiers: chr9:g.137300002C>T (hg19) ; chr9:g.134408156C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408156C>T , CM000671.2:g.134408156C>T	GRCh38
NC_000009.11:g.137300002C>T , CM000671.1:g.137300002C>T	GRCh37
NC_000009.10:g.136439823C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.287C>T MANE Select	ENSP00000419692.1:p.Ser96Leu
ENST00000672570.1:c.206C>T	ENSP00000500402.1:p.Ser69Leu
ENST00000356384.4:n.697C>T
ENST00000481739.1:c.287C>T	ENSP00000419692.1:p.Ser96Leu
NM_001291920.1:c.206C>T	NP_001278849.1:p.Ser69Leu
NM_001291921.1:c.-5C>T	NP_001278850.1:n.-5C>T
NM_002957.5:c.287C>T	NP_002948.1:p.Ser96Leu
NM_002957.6:c.287C>T MANE Select	NP_002948.1:p.Ser96Leu
NM_001291921.2:c.-5C>T	NP_001278850.1:n.-5C>T
NM_001291920.2:c.206C>T	NP_001278849.1:p.Ser69Leu