Canonical Allele Identifier: CA462128460

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103244404T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232176T>G , CM000670.2:g.102232176T>G	GRCh38
NC_000008.10:g.103244404T>G , CM000670.1:g.103244404T>G	GRCh37
NC_000008.9:g.103313580T>G	NCBI36
NG_016617.1:g.11943A>C , LRG_788:g.11943A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.177A>C MANE Select	ENSP00000251810.3:p.Ala59=
ENST00000251810.7:c.177A>C	ENSP00000251810.3:p.Ala59=
ENST00000395912.6:c.49-6142A>C	ENSP00000379248.2:n.49-6142A>C
ENST00000517517.1:n.486A>C
ENST00000519317.5:c.48+6651A>C	ENSP00000430641.1:n.48+6651A>C
ENST00000519962.5:c.48+6651A>C	ENSP00000429140.1:n.48+6651A>C
ENST00000522368.5:c.346A>C
ENST00000522394.1:c.122+55A>C	ENSP00000429578.1:n.122+55A>C
ENST00000523957.1:c.*100A>C	ENSP00000427830.1:n.*100A>C
ENST00000621845.1:c.15A>C	ENSP00000484318.1:p.Ala5=
NM_001172477.1:c.393A>C , LRG_788t1:c.393A>C	NP_001165948.1:p.Ala131=
NM_001172478.1:c.49-6142A>C	NP_001165949.1:n.49-6142A>C
NM_015713.4:c.177A>C , LRG_788t2:c.177A>C	NP_056528.2:p.Ala59=
NM_001172478.2:c.49-6142A>C	NP_001165949.1:n.49-6142A>C
NM_015713.5:c.177A>C MANE Select	NP_056528.2:p.Ala59=