Canonical Allele Identifier: CA2688143435

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102208102-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208102A>G , CM000670.2:g.102208102A>G	GRCh38
NC_000008.10:g.103220330A>G , CM000670.1:g.103220330A>G	GRCh37
NC_000008.9:g.103289506A>G	NCBI36
NG_016617.1:g.36017T>C , LRG_788:g.36017T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*31T>C MANE Select	ENSP00000251810.3:n.*31T>C
ENST00000251810.7:c.*31T>C	ENSP00000251810.3:n.*31T>C
ENST00000395910.6:n.474T>C
ENST00000522368.5:c.1256T>C
ENST00000621845.1:c.*31T>C	ENSP00000484318.1:n.*31T>C
NM_001172477.1:c.*31T>C , LRG_788t1:c.*31T>C	NP_001165948.1:n.*31T>C
NM_001172478.1:c.*31T>C	NP_001165949.1:n.*31T>C
NM_015713.4:c.*31T>C , LRG_788t2:c.*31T>C	NP_056528.2:n.*31T>C
NM_001172478.2:c.*31T>C	NP_001165949.1:n.*31T>C
NM_015713.5:c.*31T>C MANE Select	NP_056528.2:n.*31T>C