Canonical Allele Identifier: CA5172668
Gene: RAD23B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.107306580A>G , CM000671.2:g.107306580A>G GRCh38
NC_000009.11:g.110068861A>G , CM000671.1:g.110068861A>G GRCh37
NC_000009.10:g.109108682A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002874.5:c.430A>G MANE Select NP_002865.1:p.Lys144Glu
ENST00000358015.8:c.430A>G MANE Select ENSP00000350708.3:p.Lys144Glu
NM_001244713.1:c.367A>G NP_001231642.1:p.Lys123Glu
NM_001244724.1:c.214A>G NP_001231653.1:p.Lys72Glu
NM_001244724.2:c.214A>G NP_001231653.1:p.Lys72Glu
NM_002874.4:c.430A>G NP_002865.1:p.Lys144Glu
ENST00000358015.7:c.430A>G ENSP00000350708.3:p.Lys144Glu
ENST00000416373.6:c.214A>G ENSP00000405623.2:p.Lys72Glu
ENST00000419616.5:c.430A>G ENSP00000416868.1:p.Lys144Glu
ENST00000457811.1:c.39A>G