Canonical Allele Identifier: CA343472842
Gene: RXRG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.165389131C>G (hg19) chr1:g.165419894C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419894C>G , CM000663.2:g.165419894C>G GRCh38
NC_000001.10:g.165389131C>G , CM000663.1:g.165389131C>G GRCh37
NC_000001.9:g.163655755C>G NCBI36
NG_029517.1:g.30462G>C
NG_029517.2:g.30462G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.418G>C MANE Select ENSP00000352900.5:p.Ala140Pro
ENST00000359842.9:c.418G>C ENSP00000352900.5:p.Ala140Pro
ENST00000470566.1:n.343G>C
ENST00000619224.1:c.49G>C ENSP00000482458.1:p.Ala17Pro
NM_001256570.1:c.49G>C NP_001243499.1:p.Ala17Pro
NM_001256571.1:c.49G>C NP_001243500.1:p.Ala17Pro
NM_006917.4:c.418G>C NP_008848.1:p.Ala140Pro
NM_006917.5:c.418G>C MANE Select NP_008848.1:p.Ala140Pro
NM_001256571.2:c.49G>C NP_001243500.1:p.Ala17Pro
NM_001256570.2:c.49G>C NP_001243499.1:p.Ala17Pro
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