Canonical Allele Identifier: CA5317734

Gene: RXRA

Linked Data

• dbSNP Id: rs764929224
• ExAC: 9:137300157 G / C
• gnomAD v2: 9-137300157-G-C
• gnomAD v3: 9-134408311-G-C
• gnomAD v4: 9-134408311-G-C
• MyVariant Identifiers: chr9:g.137300157G>C (hg19) ; chr9:g.134408311G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408311G>C , CM000671.2:g.134408311G>C	GRCh38
NC_000009.11:g.137300157G>C , CM000671.1:g.137300157G>C	GRCh37
NC_000009.10:g.136439978G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+12G>C MANE Select	ENSP00000419692.1:n.430+12G>C
ENST00000672570.1:c.349+12G>C	ENSP00000500402.1:n.349+12G>C
ENST00000356384.4:n.840+12G>C
ENST00000481739.1:c.430+12G>C	ENSP00000419692.1:n.430+12G>C
NM_001291920.1:c.349+12G>C	NP_001278849.1:n.349+12G>C
NM_001291921.1:c.139+12G>C	NP_001278850.1:n.139+12G>C
NM_002957.5:c.430+12G>C	NP_002948.1:n.430+12G>C
NM_002957.6:c.430+12G>C MANE Select	NP_002948.1:n.430+12G>C
NM_001291921.2:c.139+12G>C	NP_001278850.1:n.139+12G>C
NM_001291920.2:c.349+12G>C	NP_001278849.1:n.349+12G>C