Canonical Allele Identifier: CA860856096

Gene: RXRA

Linked Data

• dbSNP Id: rs868316919
• MyVariant Identifiers: chr9:g.137299859G>T (hg19) ; chr9:g.134408013G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408013G>T , CM000671.2:g.134408013G>T	GRCh38
NC_000009.11:g.137299859G>T , CM000671.1:g.137299859G>T	GRCh37
NC_000009.10:g.136439680G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.280-136G>T MANE Select	ENSP00000419692.1:n.280-136G>T
ENST00000672570.1:c.199-136G>T	ENSP00000500402.1:n.199-136G>T
ENST00000356384.4:n.690-136G>T
ENST00000481739.1:c.280-136G>T	ENSP00000419692.1:n.280-136G>T
NM_001291920.1:c.199-136G>T	NP_001278849.1:n.199-136G>T
NM_001291921.1:c.-12-136G>T	NP_001278850.1:n.-12-136G>T
NM_002957.5:c.280-136G>T	NP_002948.1:n.280-136G>T
NM_002957.6:c.280-136G>T MANE Select	NP_002948.1:n.280-136G>T
NM_001291921.2:c.-12-136G>T	NP_001278850.1:n.-12-136G>T
NM_001291920.2:c.199-136G>T	NP_001278849.1:n.199-136G>T