Canonical Allele Identifier: CA343472925
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs1571275991

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419935T>G , CM000663.2:g.165419935T>G GRCh38
NC_000001.10:g.165389172T>G , CM000663.1:g.165389172T>G GRCh37
NC_000001.9:g.163655796T>G NCBI36
NG_029517.1:g.30421A>C
NG_029517.2:g.30421A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359842.10:c.377A>C MANE Select ENSP00000352900.5:p.Tyr126Ser
ENST00000359842.9:c.377A>C ENSP00000352900.5:p.Tyr126Ser
ENST00000470566.1:n.302A>C
ENST00000619224.1:c.8A>C ENSP00000482458.1:p.Tyr3Ser
NM_001256570.1:c.8A>C NP_001243499.1:p.Tyr3Ser
NM_001256571.1:c.8A>C NP_001243500.1:p.Tyr3Ser
NM_006917.4:c.377A>C NP_008848.1:p.Tyr126Ser
NM_006917.5:c.377A>C MANE Select NP_008848.1:p.Tyr126Ser
NM_001256571.2:c.8A>C NP_001243500.1:p.Tyr3Ser
NM_001256570.2:c.8A>C NP_001243499.1:p.Tyr3Ser