Canonical Allele Identifier: CA2688143441
Gene: RRM2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208119A>G , CM000670.2:g.102208119A>G GRCh38
NC_000008.10:g.103220347A>G , CM000670.1:g.103220347A>G GRCh37
NC_000008.9:g.103289523A>G NCBI36
NG_016617.1:g.36000T>C , LRG_788:g.36000T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.*14T>C MANE Select ENSP00000251810.3:n.*14T>C
ENST00000251810.7:c.*14T>C ENSP00000251810.3:n.*14T>C
ENST00000395910.6:n.457T>C
ENST00000522368.5:c.1239T>C
ENST00000621845.1:c.*14T>C ENSP00000484318.1:n.*14T>C
NM_001172477.1:c.*14T>C , LRG_788t1:c.*14T>C NP_001165948.1:n.*14T>C
NM_001172478.1:c.*14T>C NP_001165949.1:n.*14T>C
NM_015713.4:c.*14T>C , LRG_788t2:c.*14T>C NP_056528.2:n.*14T>C
NM_001172478.2:c.*14T>C NP_001165949.1:n.*14T>C
NM_015713.5:c.*14T>C MANE Select NP_056528.2:n.*14T>C