Canonical Allele Identifier: CA2688143443
Gene: RRM2B HGNC NCBI

Linked Data

gnomAD v4: 8-102208122-CGA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208126_102208127del , CM000670.2:g.102208126_102208127del GRCh38
NG_016617.1:g.35995_35996del , LRG_788:g.35995_35996del

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.*9_*10del MANE Select ENSP00000251810.3:n.*9_*10del
ENST00000251810.7:c.*9_*10del ENSP00000251810.3:n.*9_*10del
ENST00000395910.6:n.452_453del
ENST00000522368.5:c.1234_1235del
ENST00000621845.1:c.*9_*10del ENSP00000484318.1:n.*9_*10del
NM_001172477.1:c.*9_*10del , LRG_788t1:c.*9_*10del NP_001165948.1:n.*9_*10del
NM_001172478.1:c.*9_*10del NP_001165949.1:n.*9_*10del
NM_015713.4:c.*9_*10del , LRG_788t2:c.*9_*10del NP_056528.2:n.*9_*10del
NM_001172478.2:c.*9_*10del NP_001165949.1:n.*9_*10del
NM_015713.5:c.*9_*10del MANE Select NP_056528.2:n.*9_*10del
Search 100 bp 5'
Search 100 bp 3'