Canonical Allele Identifier: CA421567598
Gene: RXRG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.165389141T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419904T>C , CM000663.2:g.165419904T>C GRCh38
NC_000001.10:g.165389141T>C , CM000663.1:g.165389141T>C GRCh37
NC_000001.9:g.163655765T>C NCBI36
NG_029517.1:g.30452A>G
NG_029517.2:g.30452A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.408A>G MANE Select ENSP00000352900.5:p.Lys136=
ENST00000359842.9:c.408A>G ENSP00000352900.5:p.Lys136=
ENST00000470566.1:n.333A>G
ENST00000619224.1:c.39A>G ENSP00000482458.1:p.Lys13=
NM_001256570.1:c.39A>G NP_001243499.1:p.Lys13=
NM_001256571.1:c.39A>G NP_001243500.1:p.Lys13=
NM_006917.4:c.408A>G NP_008848.1:p.Lys136=
NM_006917.5:c.408A>G MANE Select NP_008848.1:p.Lys136=
NM_001256571.2:c.39A>G NP_001243500.1:p.Lys13=
NM_001256570.2:c.39A>G NP_001243499.1:p.Lys13=