Canonical Allele Identifier: CA10626677

Gene: RRM2B

Linked Data

• ClinVar Variation Id: 361174
• ClinVar RCV Id: RCV000337064 ; RCV000373054
• dbSNP Id: rs886062570
• gnomAD v4: 8-102208060-T-A
• MyVariant Identifiers: chr8:g.103220288T>A (hg19) ; chr8:g.102208060T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208060T>A , CM000670.2:g.102208060T>A	GRCh38
NC_000008.10:g.103220288T>A , CM000670.1:g.103220288T>A	GRCh37
NC_000008.9:g.103289464T>A	NCBI36
NG_016617.1:g.36059A>T , LRG_788:g.36059A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*73A>T MANE Select	ENSP00000251810.3:n.*73A>T
ENST00000251810.7:c.*73A>T	ENSP00000251810.3:n.*73A>T
ENST00000395910.6:n.516A>T
ENST00000522368.5:c.1298A>T
ENST00000621845.1:c.*73A>T	ENSP00000484318.1:n.*73A>T
NM_001172477.1:c.*73A>T , LRG_788t1:c.*73A>T	NP_001165948.1:n.*73A>T
NM_001172478.1:c.*73A>T	NP_001165949.1:n.*73A>T
NM_015713.4:c.*73A>T , LRG_788t2:c.*73A>T	NP_056528.2:n.*73A>T
NM_001172478.2:c.*73A>T	NP_001165949.1:n.*73A>T
NM_015713.5:c.*73A>T MANE Select	NP_056528.2:n.*73A>T