Canonical Allele Identifier: CA2688143360

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102207957-CTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102207963_102207965del , CM000670.2:g.102207963_102207965del	GRCh38
NC_000008.10:g.103220191_103220193del , CM000670.1:g.103220191_103220193del	GRCh37
NC_000008.9:g.103289367_103289369del	NCBI36
NG_016617.1:g.36159_36161del , LRG_788:g.36159_36161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*173_*175del MANE Select	ENSP00000251810.3:n.*173_*175del
ENST00000251810.7:c.*173_*175del	ENSP00000251810.3:n.*173_*175del
ENST00000395910.6:n.616_618del
ENST00000522368.5:c.1398_1400del
ENST00000621845.1:c.*173_*175del	ENSP00000484318.1:n.*173_*175del
NM_001172477.1:c.*173_*175del , LRG_788t1:c.*173_*175del	NP_001165948.1:n.*173_*175del
NM_001172478.1:c.*173_*175del	NP_001165949.1:n.*173_*175del
NM_015713.4:c.*173_*175del , LRG_788t2:c.*173_*175del	NP_056528.2:n.*173_*175del
NM_001172478.2:c.*173_*175del	NP_001165949.1:n.*173_*175del
NM_015713.5:c.*173_*175del MANE Select	NP_056528.2:n.*173_*175del