Canonical Allele Identifier: CA371586233

Gene: RRM2B

Linked Data

• dbSNP Id: rs2132539540
• MyVariant Identifiers: chr8:g.103220475G>C (hg19) ; chr8:g.102208247G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208247G>C , CM000670.2:g.102208247G>C	GRCh38
NC_000008.10:g.103220475G>C , CM000670.1:g.103220475G>C	GRCh37
NC_000008.9:g.103289651G>C	NCBI36
NG_016617.1:g.35872C>G , LRG_788:g.35872C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.942C>G MANE Select	ENSP00000251810.3:p.Asn314Lys
ENST00000251810.7:c.942C>G	ENSP00000251810.3:p.Asn314Lys
ENST00000395910.6:n.329C>G
ENST00000395912.6:c.786C>G	ENSP00000379248.2:p.Asn262Lys
ENST00000519317.5:c.306C>G	ENSP00000430641.1:p.Asn102Lys
ENST00000519962.5:c.87C>G	ENSP00000429140.1:p.Asn29Lys
ENST00000522368.5:c.1111C>G
ENST00000522394.1:c.275C>G	ENSP00000429578.1:n.275C>G
ENST00000621845.1:c.780C>G	ENSP00000484318.1:p.Asn260Lys
NM_001172477.1:c.1158C>G , LRG_788t1:c.1158C>G	NP_001165948.1:p.Asn386Lys
NM_001172478.1:c.786C>G	NP_001165949.1:p.Asn262Lys
NM_015713.4:c.942C>G , LRG_788t2:c.942C>G	NP_056528.2:p.Asn314Lys
NM_001172478.2:c.786C>G	NP_001165949.1:p.Asn262Lys
NM_015713.5:c.942C>G MANE Select	NP_056528.2:p.Asn314Lys