Canonical Allele Identifier: CA2688146592
Gene: RRM2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102219014_102219020del , CM000670.2:g.102219014_102219020del GRCh38
NC_000008.10:g.103231242_103231248del , CM000670.1:g.103231242_103231248del GRCh37
NC_000008.9:g.103300418_103300424del NCBI36
NG_016617.1:g.25099_25105del , LRG_788:g.25099_25105del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.551-73_551-67del MANE Select ENSP00000251810.3:n.551-73_551-67del
ENST00000251810.7:c.551-73_551-67del ENSP00000251810.3:n.551-73_551-67del
ENST00000395912.6:c.395-73_395-67del ENSP00000379248.2:n.395-73_395-67del
ENST00000519317.5:c.49-4862_49-4856del ENSP00000430641.1:n.49-4862_49-4856del
ENST00000519962.5:c.49-10735_49-10729del ENSP00000429140.1:n.49-10735_49-10729del
ENST00000522368.5:c.720-73_720-67del
ENST00000522394.1:c.123-6131_123-6125del ENSP00000429578.1:n.123-6131_123-6125del
ENST00000621845.1:c.389-73_389-67del ENSP00000484318.1:n.389-73_389-67del
NM_001172477.1:c.767-73_767-67del , LRG_788t1:c.767-73_767-67del NP_001165948.1:n.767-73_767-67del
NM_001172478.1:c.395-73_395-67del NP_001165949.1:n.395-73_395-67del
NM_015713.4:c.551-73_551-67del , LRG_788t2:c.551-73_551-67del NP_056528.2:n.551-73_551-67del
NM_001172478.2:c.395-73_395-67del NP_001165949.1:n.395-73_395-67del
NM_015713.5:c.551-73_551-67del MANE Select NP_056528.2:n.551-73_551-67del