Canonical Allele Identifier: CA343472787

Gene: RXRG

Linked Data

• gnomAD v4: 1-165419870-C-A
• MyVariant Identifiers: chr1:g.165389107C>A (hg19) ; chr1:g.165419870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419870C>A , CM000663.2:g.165419870C>A	GRCh38
NC_000001.10:g.165389107C>A , CM000663.1:g.165389107C>A	GRCh37
NC_000001.9:g.163655731C>A	NCBI36
NG_029517.1:g.30486G>T
NG_029517.2:g.30486G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442G>T MANE Select	ENSP00000352900.5:p.Gly148Ter
ENST00000359842.9:c.442G>T	ENSP00000352900.5:p.Gly148Ter
ENST00000470566.1:n.367G>T
ENST00000619224.1:c.73G>T	ENSP00000482458.1:p.Gly25Ter
NM_001256570.1:c.73G>T	NP_001243499.1:p.Gly25Ter
NM_001256571.1:c.73G>T	NP_001243500.1:p.Gly25Ter
NM_006917.4:c.442G>T	NP_008848.1:p.Gly148Ter
NM_006917.5:c.442G>T MANE Select	NP_008848.1:p.Gly148Ter
NM_001256571.2:c.73G>T	NP_001243500.1:p.Gly25Ter
NM_001256570.2:c.73G>T	NP_001243499.1:p.Gly25Ter