Canonical Allele Identifier: CA371586085

Gene: RRM2B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.958A>T MANE Select	ENSP00000251810.3:p.Lys320Ter
ENST00000251810.7:c.958A>T	ENSP00000251810.3:p.Lys320Ter
ENST00000395910.6:n.345A>T
ENST00000395912.6:c.802A>T	ENSP00000379248.2:p.Lys268Ter
ENST00000519317.5:c.322A>T	ENSP00000430641.1:p.Lys108Ter
ENST00000519962.5:c.103A>T	ENSP00000429140.1:p.Lys35Ter
ENST00000522368.5:c.1127A>T
ENST00000522394.1:c.291A>T	ENSP00000429578.1:n.291A>T
ENST00000621845.1:c.796A>T	ENSP00000484318.1:p.Lys266Ter
NM_001172477.1:c.1174A>T , LRG_788t1:c.1174A>T	NP_001165948.1:p.Lys392Ter
NM_001172478.1:c.802A>T	NP_001165949.1:p.Lys268Ter
NM_015713.4:c.958A>T , LRG_788t2:c.958A>T	NP_056528.2:p.Lys320Ter
NM_001172478.2:c.802A>T	NP_001165949.1:p.Lys268Ter
NM_015713.5:c.958A>T MANE Select	NP_056528.2:p.Lys320Ter