Canonical Allele Identifier: CA1806674655
Gene: RRM2B HGNC NCBI

Linked Data

dbSNP Id: rs1265117
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208123G>C , CM000670.2:g.102208123G>C GRCh38
NG_016617.1:g.35996C>G , LRG_788:g.35996C>G

Transcript Alleles

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