Canonical Allele Identifier: CA345570
Gene: RRM2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102225020T>G , CM000670.2:g.102225020T>G GRCh38
NC_000008.10:g.103237248T>G , CM000670.1:g.103237248T>G GRCh37
NC_000008.9:g.103306424T>G NCBI36
NG_016617.1:g.19099A>C , LRG_788:g.19099A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.322-2A>C MANE Select ENSP00000251810.3:n.322-2A>C
ENST00000251810.7:c.322-2A>C ENSP00000251810.3:n.322-2A>C
ENST00000395912.6:c.166-2A>C ENSP00000379248.2:n.166-2A>C
ENST00000519317.5:c.49-10862A>C ENSP00000430641.1:n.49-10862A>C
ENST00000519962.5:c.48+13807A>C ENSP00000429140.1:n.48+13807A>C
ENST00000522368.5:c.491-2A>C
ENST00000522394.1:c.122+7211A>C ENSP00000429578.1:n.122+7211A>C
ENST00000523957.1:c.*245-2A>C ENSP00000427830.1:n.*245-2A>C
ENST00000621845.1:c.160-2A>C ENSP00000484318.1:n.160-2A>C
NM_001172477.1:c.538-2A>C , LRG_788t1:c.538-2A>C NP_001165948.1:n.538-2A>C
NM_001172478.1:c.166-2A>C NP_001165949.1:n.166-2A>C
NM_015713.4:c.322-2A>C , LRG_788t2:c.322-2A>C NP_056528.2:n.322-2A>C
NM_001172478.2:c.166-2A>C NP_001165949.1:n.166-2A>C
NM_015713.5:c.322-2A>C MANE Select NP_056528.2:n.322-2A>C
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