Canonical Allele Identifier: CA1139919773
Community Standard Title: NM_006917.5(RXRG):c.49+3297T=
Gene: RXRG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165441548A= , CM000663.2:g.165441548A= GRCh38
NC_000001.10:g.165410785A= , CM000663.1:g.165410785A= GRCh37
NC_000001.9:g.163677409A= NCBI36
NG_029517.1:g.8808T=
NG_029517.2:g.8808T=

Transcript Alleles

HGVS Amino-acid Change
NM_006917.5:c.49+3297T= MANE Select NP_008848.1:n.49+3297T=
ENST00000359842.10:c.49+3297T= MANE Select ENSP00000352900.5:n.49+3297T=
NM_001256570.1:c.-379+3297T= NP_001243499.1:n.-379+3297T=
NM_001256570.2:c.-379+3297T= NP_001243499.1:n.-379+3297T=
NM_006917.4:c.49+3297T= NP_008848.1:n.49+3297T=
NR_033824.1:n.511+3297T=
NR_033824.2:n.282+3297T=
ENST00000359842.9:c.49+3297T= ENSP00000352900.5:n.49+3297T=
ENST00000465764.1:n.328+3297T=
ENST00000619224.1:c.-379+3297T= ENSP00000482458.1:n.-379+3297T=