Canonical Allele Identifier: CA371593153

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237213C>G (hg19) ; chr8:g.102224985C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224985C>G , CM000670.2:g.102224985C>G	GRCh38
NC_000008.10:g.103237213C>G , CM000670.1:g.103237213C>G	GRCh37
NC_000008.9:g.103306389C>G	NCBI36
NG_016617.1:g.19134G>C , LRG_788:g.19134G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.355G>C MANE Select	ENSP00000251810.3:p.Glu119Gln
ENST00000251810.7:c.355G>C	ENSP00000251810.3:p.Glu119Gln
ENST00000395912.6:c.199G>C	ENSP00000379248.2:p.Glu67Gln
ENST00000519317.5:c.49-10827G>C	ENSP00000430641.1:n.49-10827G>C
ENST00000519962.5:c.48+13842G>C	ENSP00000429140.1:n.48+13842G>C
ENST00000522368.5:c.524G>C
ENST00000522394.1:c.122+7246G>C	ENSP00000429578.1:n.122+7246G>C
ENST00000523957.1:c.*278G>C	ENSP00000427830.1:n.*278G>C
ENST00000621845.1:c.193G>C	ENSP00000484318.1:p.Glu65Gln
NM_001172477.1:c.571G>C , LRG_788t1:c.571G>C	NP_001165948.1:p.Glu191Gln
NM_001172478.1:c.199G>C	NP_001165949.1:p.Glu67Gln
NM_015713.4:c.355G>C , LRG_788t2:c.355G>C	NP_056528.2:p.Glu119Gln
NM_001172478.2:c.199G>C	NP_001165949.1:p.Glu67Gln
NM_015713.5:c.355G>C MANE Select	NP_056528.2:p.Glu119Gln