Canonical Allele Identifier: CA371586096

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220459T>G (hg19) ; chr8:g.102208231T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208231T>G , CM000670.2:g.102208231T>G	GRCh38
NC_000008.10:g.103220459T>G , CM000670.1:g.103220459T>G	GRCh37
NC_000008.9:g.103289635T>G	NCBI36
NG_016617.1:g.35888A>C , LRG_788:g.35888A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.958A>C MANE Select	ENSP00000251810.3:p.Lys320Gln
ENST00000251810.7:c.958A>C	ENSP00000251810.3:p.Lys320Gln
ENST00000395910.6:n.345A>C
ENST00000395912.6:c.802A>C	ENSP00000379248.2:p.Lys268Gln
ENST00000519317.5:c.322A>C	ENSP00000430641.1:p.Lys108Gln
ENST00000519962.5:c.103A>C	ENSP00000429140.1:p.Lys35Gln
ENST00000522368.5:c.1127A>C
ENST00000522394.1:c.291A>C	ENSP00000429578.1:n.291A>C
ENST00000621845.1:c.796A>C	ENSP00000484318.1:p.Lys266Gln
NM_001172477.1:c.1174A>C , LRG_788t1:c.1174A>C	NP_001165948.1:p.Lys392Gln
NM_001172478.1:c.802A>C	NP_001165949.1:p.Lys268Gln
NM_015713.4:c.958A>C , LRG_788t2:c.958A>C	NP_056528.2:p.Lys320Gln
NM_001172478.2:c.802A>C	NP_001165949.1:p.Lys268Gln
NM_015713.5:c.958A>C MANE Select	NP_056528.2:p.Lys320Gln