Canonical Allele Identifier: CA2688143366
Gene: RRM2B HGNC NCBI

Linked Data

gnomAD v4: 8-102207972-GA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102207976del , CM000670.2:g.102207976del GRCh38
NC_000008.10:g.103220204del , CM000670.1:g.103220204del GRCh37
NC_000008.9:g.103289380del NCBI36
NG_016617.1:g.36146del , LRG_788:g.36146del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.*160del MANE Select ENSP00000251810.3:n.*160del
ENST00000251810.7:c.*160del ENSP00000251810.3:n.*160del
ENST00000395910.6:n.603del
ENST00000522368.5:c.1385del
ENST00000621845.1:c.*160del ENSP00000484318.1:n.*160del
NM_001172477.1:c.*160del , LRG_788t1:c.*160del NP_001165948.1:n.*160del
NM_001172478.1:c.*160del NP_001165949.1:n.*160del
NM_015713.4:c.*160del , LRG_788t2:c.*160del NP_056528.2:n.*160del
NM_001172478.2:c.*160del NP_001165949.1:n.*160del
NM_015713.5:c.*160del MANE Select NP_056528.2:n.*160del
Search 100 bp 5'
Search 100 bp 3'