Canonical Allele Identifier: CA371595915

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232178C>G , CM000670.2:g.102232178C>G	GRCh38
NC_000008.10:g.103244406C>G , CM000670.1:g.103244406C>G	GRCh37
NC_000008.9:g.103313582C>G	NCBI36
NG_016617.1:g.11941G>C , LRG_788:g.11941G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.175G>C MANE Select	ENSP00000251810.3:p.Ala59Pro
ENST00000251810.7:c.175G>C	ENSP00000251810.3:p.Ala59Pro
ENST00000395912.6:c.49-6144G>C	ENSP00000379248.2:n.49-6144G>C
ENST00000517517.1:n.484G>C
ENST00000519317.5:c.48+6649G>C	ENSP00000430641.1:n.48+6649G>C
ENST00000519962.5:c.48+6649G>C	ENSP00000429140.1:n.48+6649G>C
ENST00000522368.5:c.344G>C
ENST00000522394.1:c.122+53G>C	ENSP00000429578.1:n.122+53G>C
ENST00000523957.1:c.*98G>C	ENSP00000427830.1:n.*98G>C
ENST00000621845.1:c.13G>C	ENSP00000484318.1:p.Ala5Pro
NM_001172477.1:c.391G>C , LRG_788t1:c.391G>C	NP_001165948.1:p.Ala131Pro
NM_001172478.1:c.49-6144G>C	NP_001165949.1:n.49-6144G>C
NM_015713.4:c.175G>C , LRG_788t2:c.175G>C	NP_056528.2:p.Ala59Pro
NM_001172478.2:c.49-6144G>C	NP_001165949.1:n.49-6144G>C
NM_015713.5:c.175G>C MANE Select	NP_056528.2:p.Ala59Pro