Canonical Allele Identifier: CA32223409

Gene: RXRG

Linked Data

• dbSNP Id: rs775186464
• gnomAD v3: 1-165439831-G-T
• gnomAD v4: 1-165439831-G-T
• MyVariant Identifiers: chr1:g.165409068G>T (hg19) ; chr1:g.165439831G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439831G>T , CM000663.2:g.165439831G>T	GRCh38
NC_000001.10:g.165409068G>T , CM000663.1:g.165409068G>T	GRCh37
NC_000001.9:g.163675692G>T	NCBI36
NG_029517.1:g.10525C>A
NG_029517.2:g.10525C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+5014C>A MANE Select	ENSP00000352900.5:n.49+5014C>A
ENST00000359842.9:c.49+5014C>A	ENSP00000352900.5:n.49+5014C>A
ENST00000465764.1:n.329-2630C>A
ENST00000619224.1:c.-379+5014C>A	ENSP00000482458.1:n.-379+5014C>A
NM_001256570.1:c.-379+5014C>A	NP_001243499.1:n.-379+5014C>A
NM_006917.4:c.49+5014C>A	NP_008848.1:n.49+5014C>A
NR_033824.1:n.512-2630C>A
NM_006917.5:c.49+5014C>A MANE Select	NP_008848.1:n.49+5014C>A
NR_033824.2:n.283-2630C>A
NM_001256570.2:c.-379+5014C>A	NP_001243499.1:n.-379+5014C>A