Canonical Allele Identifier: CA2688143399

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102208028-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208033dup , CM000670.2:g.102208033dup	GRCh38
NC_000008.10:g.103220261dup , CM000670.1:g.103220261dup	GRCh37
NC_000008.9:g.103289437dup	NCBI36
NG_016617.1:g.36090dup , LRG_788:g.36090dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*104dup MANE Select	ENSP00000251810.3:n.*104dup
ENST00000251810.7:c.*104dup	ENSP00000251810.3:n.*104dup
ENST00000395910.6:n.547dup
ENST00000522368.5:c.1329dup
ENST00000621845.1:c.*104dup	ENSP00000484318.1:n.*104dup
NM_001172477.1:c.*104dup , LRG_788t1:c.*104dup	NP_001165948.1:n.*104dup
NM_001172478.1:c.*104dup	NP_001165949.1:n.*104dup
NM_015713.4:c.*104dup , LRG_788t2:c.*104dup	NP_056528.2:n.*104dup
NM_001172478.2:c.*104dup	NP_001165949.1:n.*104dup
NM_015713.5:c.*104dup MANE Select	NP_056528.2:n.*104dup