Canonical Allele Identifier: CA32223419

Gene: RXRG

Linked Data

• dbSNP Id: rs375783248
• gnomAD v3: 1-165439937-T-G
• gnomAD v4: 1-165439937-T-G
• MyVariant Identifiers: chr1:g.165409174T>G (hg19) ; chr1:g.165439937T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439937T>G , CM000663.2:g.165439937T>G	GRCh38
NC_000001.10:g.165409174T>G , CM000663.1:g.165409174T>G	GRCh37
NC_000001.9:g.163675798T>G	NCBI36
NG_029517.1:g.10419A>C
NG_029517.2:g.10419A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4908A>C MANE Select	ENSP00000352900.5:n.49+4908A>C
ENST00000359842.9:c.49+4908A>C	ENSP00000352900.5:n.49+4908A>C
ENST00000465764.1:n.329-2736A>C
ENST00000619224.1:c.-379+4908A>C	ENSP00000482458.1:n.-379+4908A>C
NM_001256570.1:c.-379+4908A>C	NP_001243499.1:n.-379+4908A>C
NM_006917.4:c.49+4908A>C	NP_008848.1:n.49+4908A>C
NR_033824.1:n.512-2736A>C
NM_006917.5:c.49+4908A>C MANE Select	NP_008848.1:n.49+4908A>C
NR_033824.2:n.283-2736A>C
NM_001256570.2:c.-379+4908A>C	NP_001243499.1:n.-379+4908A>C