Canonical Allele Identifier: CA2688143387

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102208014-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208014T>C , CM000670.2:g.102208014T>C	GRCh38
NC_000008.10:g.103220242T>C , CM000670.1:g.103220242T>C	GRCh37
NC_000008.9:g.103289418T>C	NCBI36
NG_016617.1:g.36105A>G , LRG_788:g.36105A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*119A>G MANE Select	ENSP00000251810.3:n.*119A>G
ENST00000251810.7:c.*119A>G	ENSP00000251810.3:n.*119A>G
ENST00000395910.6:n.562A>G
ENST00000522368.5:c.1344A>G
ENST00000621845.1:c.*119A>G	ENSP00000484318.1:n.*119A>G
NM_001172477.1:c.*119A>G , LRG_788t1:c.*119A>G	NP_001165948.1:n.*119A>G
NM_001172478.1:c.*119A>G	NP_001165949.1:n.*119A>G
NM_015713.4:c.*119A>G , LRG_788t2:c.*119A>G	NP_056528.2:n.*119A>G
NM_001172478.2:c.*119A>G	NP_001165949.1:n.*119A>G
NM_015713.5:c.*119A>G MANE Select	NP_056528.2:n.*119A>G