Canonical Allele Identifier: CA1806674654
Gene: RRM2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208122_102208123delinsCG , CM000670.2:g.102208122_102208123delinsCG GRCh38
NG_016617.1:g.35996_35997delinsCG , LRG_788:g.35996_35997delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.*10_*11delinsCG MANE Select ENSP00000251810.3:n.*10_*11delinsCG
ENST00000251810.7:c.*10_*11delinsCG ENSP00000251810.3:n.*10_*11delinsCG
ENST00000395910.6:n.453_454delinsCG
ENST00000522368.5:c.1235_1236delinsCG
ENST00000621845.1:c.*10_*11delinsCG ENSP00000484318.1:n.*10_*11delinsCG
NM_001172477.1:c.*10_*11delinsCG , LRG_788t1:c.*10_*11delinsCG NP_001165948.1:n.*10_*11delinsCG
NM_001172478.1:c.*10_*11delinsCG NP_001165949.1:n.*10_*11delinsCG
NM_015713.4:c.*10_*11delinsCG , LRG_788t2:c.*10_*11delinsCG NP_056528.2:n.*10_*11delinsCG
NM_001172478.2:c.*10_*11delinsCG NP_001165949.1:n.*10_*11delinsCG
NM_015713.5:c.*10_*11delinsCG MANE Select NP_056528.2:n.*10_*11delinsCG
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