Canonical Allele Identifier: CA890557464

Gene: RXRG

Linked Data

• dbSNP Id: rs1399435998
• gnomAD v3: 1-165439729-A-C
• gnomAD v4: 1-165439729-A-C
• MyVariant Identifiers: chr1:g.165408966A>C (hg19) ; chr1:g.165439729A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439729A>C , CM000663.2:g.165439729A>C	GRCh38
NC_000001.10:g.165408966A>C , CM000663.1:g.165408966A>C	GRCh37
NC_000001.9:g.163675590A>C	NCBI36
NG_029517.1:g.10627T>G
NG_029517.2:g.10627T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+5116T>G MANE Select	ENSP00000352900.5:n.49+5116T>G
ENST00000359842.9:c.49+5116T>G	ENSP00000352900.5:n.49+5116T>G
ENST00000465764.1:n.329-2528T>G
ENST00000619224.1:c.-379+5116T>G	ENSP00000482458.1:n.-379+5116T>G
NM_001256570.1:c.-379+5116T>G	NP_001243499.1:n.-379+5116T>G
NM_006917.4:c.49+5116T>G	NP_008848.1:n.49+5116T>G
NR_033824.1:n.512-2528T>G
NM_006917.5:c.49+5116T>G MANE Select	NP_008848.1:n.49+5116T>G
NR_033824.2:n.283-2528T>G
NM_001256570.2:c.-379+5116T>G	NP_001243499.1:n.-379+5116T>G