Canonical Allele Identifier: CA371596025

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103244420T>G (hg19) ; chr8:g.102232192T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232192T>G , CM000670.2:g.102232192T>G	GRCh38
NC_000008.10:g.103244420T>G , CM000670.1:g.103244420T>G	GRCh37
NC_000008.9:g.103313596T>G	NCBI36
NG_016617.1:g.11927A>C , LRG_788:g.11927A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.161A>C MANE Select	ENSP00000251810.3:p.Lys54Thr
ENST00000251810.7:c.161A>C	ENSP00000251810.3:p.Lys54Thr
ENST00000395912.6:c.49-6158A>C	ENSP00000379248.2:n.49-6158A>C
ENST00000517517.1:n.470A>C
ENST00000519317.5:c.48+6635A>C	ENSP00000430641.1:n.48+6635A>C
ENST00000519962.5:c.48+6635A>C	ENSP00000429140.1:n.48+6635A>C
ENST00000522368.5:c.330A>C
ENST00000522394.1:c.122+39A>C	ENSP00000429578.1:n.122+39A>C
ENST00000523957.1:c.*84A>C	ENSP00000427830.1:n.*84A>C
ENST00000621845.1:c.-2A>C	ENSP00000484318.1:n.-2A>C
NM_001172477.1:c.377A>C , LRG_788t1:c.377A>C	NP_001165948.1:p.Lys126Thr
NM_001172478.1:c.49-6158A>C	NP_001165949.1:n.49-6158A>C
NM_015713.4:c.161A>C , LRG_788t2:c.161A>C	NP_056528.2:p.Lys54Thr
NM_001172478.2:c.49-6158A>C	NP_001165949.1:n.49-6158A>C
NM_015713.5:c.161A>C MANE Select	NP_056528.2:p.Lys54Thr