Canonical Allele Identifier: CA421567627

Gene: RXRG

Linked Data

• dbSNP Id: rs1168957429
• gnomAD v2: 1-165389171-G-A
• gnomAD v4: 1-165419934-G-A
• MyVariant Identifiers: chr1:g.165389171G>A (hg19) ; chr1:g.165419934G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419934G>A , CM000663.2:g.165419934G>A	GRCh38
NC_000001.10:g.165389171G>A , CM000663.1:g.165389171G>A	GRCh37
NC_000001.9:g.163655795G>A	NCBI36
NG_029517.1:g.30422C>T
NG_029517.2:g.30422C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.378C>T MANE Select	ENSP00000352900.5:p.Tyr126=
ENST00000359842.9:c.378C>T	ENSP00000352900.5:p.Tyr126=
ENST00000470566.1:n.303C>T
ENST00000619224.1:c.9C>T	ENSP00000482458.1:p.Tyr3=
NM_001256570.1:c.9C>T	NP_001243499.1:p.Tyr3=
NM_001256571.1:c.9C>T	NP_001243500.1:p.Tyr3=
NM_006917.4:c.378C>T	NP_008848.1:p.Tyr126=
NM_006917.5:c.378C>T MANE Select	NP_008848.1:p.Tyr126=
NM_001256571.2:c.9C>T	NP_001243500.1:p.Tyr3=
NM_001256570.2:c.9C>T	NP_001243499.1:p.Tyr3=