Canonical Allele Identifier: CA371593169

Gene: RRM2B

Linked Data

• dbSNP Id: rs1810904555
• MyVariant Identifiers: chr8:g.103237218A>T (hg19) ; chr8:g.102224990A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224990A>T , CM000670.2:g.102224990A>T	GRCh38
NC_000008.10:g.103237218A>T , CM000670.1:g.103237218A>T	GRCh37
NC_000008.9:g.103306394A>T	NCBI36
NG_016617.1:g.19129T>A , LRG_788:g.19129T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.350T>A MANE Select	ENSP00000251810.3:p.Val117Asp
ENST00000251810.7:c.350T>A	ENSP00000251810.3:p.Val117Asp
ENST00000395912.6:c.194T>A	ENSP00000379248.2:p.Val65Asp
ENST00000519317.5:c.49-10832T>A	ENSP00000430641.1:n.49-10832T>A
ENST00000519962.5:c.48+13837T>A	ENSP00000429140.1:n.48+13837T>A
ENST00000522368.5:c.519T>A
ENST00000522394.1:c.122+7241T>A	ENSP00000429578.1:n.122+7241T>A
ENST00000523957.1:c.*273T>A	ENSP00000427830.1:n.*273T>A
ENST00000621845.1:c.188T>A	ENSP00000484318.1:p.Val63Asp
NM_001172477.1:c.566T>A , LRG_788t1:c.566T>A	NP_001165948.1:p.Val189Asp
NM_001172478.1:c.194T>A	NP_001165949.1:p.Val65Asp
NM_015713.4:c.350T>A , LRG_788t2:c.350T>A	NP_056528.2:p.Val117Asp
NM_001172478.2:c.194T>A	NP_001165949.1:p.Val65Asp
NM_015713.5:c.350T>A MANE Select	NP_056528.2:p.Val117Asp