Canonical Allele Identifier: CA32223413

Gene: RXRG

Linked Data

• dbSNP Id: rs764650534
• gnomAD v2: 1-165409101-C-A
• gnomAD v3: 1-165439864-C-A
• gnomAD v4: 1-165439864-C-A
• MyVariant Identifiers: chr1:g.165409101C>A (hg19) ; chr1:g.165439864C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439864C>A , CM000663.2:g.165439864C>A	GRCh38
NC_000001.10:g.165409101C>A , CM000663.1:g.165409101C>A	GRCh37
NC_000001.9:g.163675725C>A	NCBI36
NG_029517.1:g.10492G>T
NG_029517.2:g.10492G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359842.10:c.49+4981G>T MANE Select	ENSP00000352900.5:n.49+4981G>T
ENST00000359842.9:c.49+4981G>T	ENSP00000352900.5:n.49+4981G>T
ENST00000465764.1:n.329-2663G>T
ENST00000619224.1:c.-379+4981G>T	ENSP00000482458.1:n.-379+4981G>T
NM_001256570.1:c.-379+4981G>T	NP_001243499.1:n.-379+4981G>T
NM_006917.4:c.49+4981G>T	NP_008848.1:n.49+4981G>T
NR_033824.1:n.512-2663G>T
NM_006917.5:c.49+4981G>T MANE Select	NP_008848.1:n.49+4981G>T
NR_033824.2:n.283-2663G>T
NM_001256570.2:c.-379+4981G>T	NP_001243499.1:n.-379+4981G>T