Canonical Allele Identifier: CA1806674652
Gene: RRM2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208121_102208123delinsACG , CM000670.2:g.102208121_102208123delinsACG GRCh38
NG_016617.1:g.35996_35998delinsCGT , LRG_788:g.35996_35998delinsCGT

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.*10_*12delinsCGT MANE Select ENSP00000251810.3:n.*10_*12delinsCGT
ENST00000251810.7:c.*10_*12delinsCGT ENSP00000251810.3:n.*10_*12delinsCGT
ENST00000395910.6:n.453_455delinsCGT
ENST00000522368.5:c.1235_1237delinsCGT
ENST00000621845.1:c.*10_*12delinsCGT ENSP00000484318.1:n.*10_*12delinsCGT
NM_001172477.1:c.*10_*12delinsCGT , LRG_788t1:c.*10_*12delinsCGT NP_001165948.1:n.*10_*12delinsCGT
NM_001172478.1:c.*10_*12delinsCGT NP_001165949.1:n.*10_*12delinsCGT
NM_015713.4:c.*10_*12delinsCGT , LRG_788t2:c.*10_*12delinsCGT NP_056528.2:n.*10_*12delinsCGT
NM_001172478.2:c.*10_*12delinsCGT NP_001165949.1:n.*10_*12delinsCGT
NM_015713.5:c.*10_*12delinsCGT MANE Select NP_056528.2:n.*10_*12delinsCGT
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