Canonical Allele Identifier: CA890586099

Gene: RXRG

Linked Data

• dbSNP Id: rs1393233094
• gnomAD v3: 1-165419749-G-C
• gnomAD v4: 1-165419749-G-C
• MyVariant Identifiers: chr1:g.165388986G>C (hg19) ; chr1:g.165419749G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419749G>C , CM000663.2:g.165419749G>C	GRCh38
NC_000001.10:g.165388986G>C , CM000663.1:g.165388986G>C	GRCh37
NC_000001.9:g.163655610G>C	NCBI36
NG_029517.1:g.30607C>G
NG_029517.2:g.30607C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+121C>G MANE Select	ENSP00000352900.5:n.442+121C>G
ENST00000359842.9:c.442+121C>G	ENSP00000352900.5:n.442+121C>G
ENST00000470566.1:n.367+121C>G
ENST00000619224.1:c.73+121C>G	ENSP00000482458.1:n.73+121C>G
NM_001256570.1:c.73+121C>G	NP_001243499.1:n.73+121C>G
NM_001256571.1:c.73+121C>G	NP_001243500.1:n.73+121C>G
NM_006917.4:c.442+121C>G	NP_008848.1:n.442+121C>G
NM_006917.5:c.442+121C>G MANE Select	NP_008848.1:n.442+121C>G
NM_001256571.2:c.73+121C>G	NP_001243500.1:n.73+121C>G
NM_001256570.2:c.73+121C>G	NP_001243499.1:n.73+121C>G