Canonical Allele Identifier: CA462123677

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220397G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208169G>A , CM000670.2:g.102208169G>A	GRCh38
NC_000008.10:g.103220397G>A , CM000670.1:g.103220397G>A	GRCh37
NC_000008.9:g.103289573G>A	NCBI36
NG_016617.1:g.35950C>T , LRG_788:g.35950C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1020C>T MANE Select	ENSP00000251810.3:p.Thr340=
ENST00000251810.7:c.1020C>T	ENSP00000251810.3:p.Thr340=
ENST00000395910.6:n.407C>T
ENST00000395912.6:c.864C>T	ENSP00000379248.2:p.Thr288=
ENST00000519317.5:c.384C>T	ENSP00000430641.1:p.Thr128=
ENST00000519962.5:c.165C>T	ENSP00000429140.1:p.Thr55=
ENST00000522368.5:c.1189C>T
ENST00000522394.1:c.353C>T	ENSP00000429578.1:n.353C>T
ENST00000621845.1:c.858C>T	ENSP00000484318.1:p.Thr286=
NM_001172477.1:c.1236C>T , LRG_788t1:c.1236C>T	NP_001165948.1:p.Thr412=
NM_001172478.1:c.864C>T	NP_001165949.1:p.Thr288=
NM_015713.4:c.1020C>T , LRG_788t2:c.1020C>T	NP_056528.2:p.Thr340=
NM_001172478.2:c.864C>T	NP_001165949.1:p.Thr288=
NM_015713.5:c.1020C>T MANE Select	NP_056528.2:p.Thr340=