Canonical Allele Identifier: CA1806674608

Gene: RRM2B

Linked Data

• dbSNP Id: rs1810572390

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102207994_102207997del , CM000670.2:g.102207994_102207997del	GRCh38
NC_000008.10:g.103220222_103220225del , CM000670.1:g.103220222_103220225del	GRCh37
NC_000008.9:g.103289398_103289401del	NCBI36
NG_016617.1:g.36124_36127del , LRG_788:g.36124_36127del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*138_*141del MANE Select	ENSP00000251810.3:n.*138_*141del
ENST00000251810.7:c.*138_*141del	ENSP00000251810.3:n.*138_*141del
ENST00000395910.6:n.581_584del
ENST00000522368.5:c.1363_1366del
ENST00000621845.1:c.*138_*141del	ENSP00000484318.1:n.*138_*141del
NM_001172477.1:c.*138_*141del , LRG_788t1:c.*138_*141del	NP_001165948.1:n.*138_*141del
NM_001172478.1:c.*138_*141del	NP_001165949.1:n.*138_*141del
NM_015713.4:c.*138_*141del , LRG_788t2:c.*138_*141del	NP_056528.2:n.*138_*141del
NM_001172478.2:c.*138_*141del	NP_001165949.1:n.*138_*141del
NM_015713.5:c.*138_*141del MANE Select	NP_056528.2:n.*138_*141del