Canonical Allele Identifier: CA1806674627
Gene: RRM2B HGNC NCBI

Linked Data

dbSNP Id: rs1810573221
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208052del , CM000670.2:g.102208052del GRCh38
NC_000008.10:g.103220280del , CM000670.1:g.103220280del GRCh37
NC_000008.9:g.103289456del NCBI36
NG_016617.1:g.36067del , LRG_788:g.36067del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.*81del MANE Select ENSP00000251810.3:n.*81del
ENST00000251810.7:c.*81del ENSP00000251810.3:n.*81del
ENST00000395910.6:n.524del
ENST00000522368.5:c.1306del
ENST00000621845.1:c.*81del ENSP00000484318.1:n.*81del
NM_001172477.1:c.*81del , LRG_788t1:c.*81del NP_001165948.1:n.*81del
NM_001172478.1:c.*81del NP_001165949.1:n.*81del
NM_015713.4:c.*81del , LRG_788t2:c.*81del NP_056528.2:n.*81del
NM_001172478.2:c.*81del NP_001165949.1:n.*81del
NM_015713.5:c.*81del MANE Select NP_056528.2:n.*81del
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