Canonical Allele Identifier: CA4831065
Gene: RRM2B HGNC NCBI

Linked Data

dbSNP Id: rs750186733

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102218996T>A , CM000670.2:g.102218996T>A GRCh38
NC_000008.10:g.103231224T>A , CM000670.1:g.103231224T>A GRCh37
NC_000008.9:g.103300400T>A NCBI36
NG_016617.1:g.25123A>T , LRG_788:g.25123A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.551-49A>T MANE Select ENSP00000251810.3:n.551-49A>T
ENST00000251810.7:c.551-49A>T ENSP00000251810.3:n.551-49A>T
ENST00000395912.6:c.395-49A>T ENSP00000379248.2:n.395-49A>T
ENST00000519125.1:n.20A>T
ENST00000519317.5:c.49-4838A>T ENSP00000430641.1:n.49-4838A>T
ENST00000519962.5:c.49-10711A>T ENSP00000429140.1:n.49-10711A>T
ENST00000522368.5:c.720-49A>T
ENST00000522394.1:c.123-6107A>T ENSP00000429578.1:n.123-6107A>T
ENST00000621845.1:c.389-49A>T ENSP00000484318.1:n.389-49A>T
NM_001172477.1:c.767-49A>T , LRG_788t1:c.767-49A>T NP_001165948.1:n.767-49A>T
NM_001172478.1:c.395-49A>T NP_001165949.1:n.395-49A>T
NM_015713.4:c.551-49A>T , LRG_788t2:c.551-49A>T NP_056528.2:n.551-49A>T
NM_001172478.2:c.395-49A>T NP_001165949.1:n.395-49A>T
NM_015713.5:c.551-49A>T MANE Select NP_056528.2:n.551-49A>T