Canonical Allele Identifier: CA2579221157
Gene: RRM2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208112_102208113del , CM000670.2:g.102208112_102208113del GRCh38
NC_000008.10:g.103220340_103220341del , CM000670.1:g.103220340_103220341del GRCh37
NC_000008.9:g.103289516_103289517del NCBI36
NG_016617.1:g.36008_36009del , LRG_788:g.36008_36009del

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.*22_*23del MANE Select ENSP00000251810.3:n.*22_*23del
ENST00000251810.7:c.*22_*23del ENSP00000251810.3:n.*22_*23del
ENST00000395910.6:n.465_466del
ENST00000522368.5:c.1247_1248del
ENST00000621845.1:c.*22_*23del ENSP00000484318.1:n.*22_*23del
NM_001172477.1:c.*22_*23del , LRG_788t1:c.*22_*23del NP_001165948.1:n.*22_*23del
NM_001172478.1:c.*22_*23del NP_001165949.1:n.*22_*23del
NM_015713.4:c.*22_*23del , LRG_788t2:c.*22_*23del NP_056528.2:n.*22_*23del
NM_001172478.2:c.*22_*23del NP_001165949.1:n.*22_*23del
NM_015713.5:c.*22_*23del MANE Select NP_056528.2:n.*22_*23del