Canonical Allele Identifier: CA1220190
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs771801335

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419861del , CM000663.2:g.165419861del GRCh38
NC_000001.10:g.165389098del , CM000663.1:g.165389098del GRCh37
NC_000001.9:g.163655722del NCBI36
NG_029517.1:g.30495del
NG_029517.2:g.30495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.442+9del MANE Select ENSP00000352900.5:n.442+9del
ENST00000359842.9:c.442+9del ENSP00000352900.5:n.442+9del
ENST00000470566.1:n.367+9del
ENST00000619224.1:c.73+9del ENSP00000482458.1:n.73+9del
NM_001256570.1:c.73+9del NP_001243499.1:n.73+9del
NM_001256571.1:c.73+9del NP_001243500.1:n.73+9del
NM_006917.4:c.442+9del NP_008848.1:n.442+9del
NM_006917.5:c.442+9del MANE Select NP_008848.1:n.442+9del
NM_001256571.2:c.73+9del NP_001243500.1:n.73+9del
NM_001256570.2:c.73+9del NP_001243499.1:n.73+9del