Canonical Allele Identifier: CA1204410116
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419871T= , CM000663.2:g.165419871T= GRCh38
NC_000001.10:g.165389108T= , CM000663.1:g.165389108T= GRCh37
NC_000001.9:g.163655732T= NCBI36
NG_029517.1:g.30485A=
NG_029517.2:g.30485A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.441A= MANE Select ENSP00000352900.5:p.Ser147=
ENST00000359842.9:c.441A= ENSP00000352900.5:p.Ser147=
ENST00000470566.1:n.366A=
ENST00000619224.1:c.72A= ENSP00000482458.1:p.Ser24=
NM_001256570.1:c.72A= NP_001243499.1:p.Ser24=
NM_001256571.1:c.72A= NP_001243500.1:p.Ser24=
NM_006917.4:c.441A= NP_008848.1:p.Ser147=
NM_006917.5:c.441A= MANE Select NP_008848.1:p.Ser147=
NM_001256571.2:c.72A= NP_001243500.1:p.Ser24=
NM_001256570.2:c.72A= NP_001243499.1:p.Ser24=