Canonical Allele Identifier: CA462123655

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220370T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208142T>A , CM000670.2:g.102208142T>A	GRCh38
NC_000008.10:g.103220370T>A , CM000670.1:g.103220370T>A	GRCh37
NC_000008.9:g.103289546T>A	NCBI36
NG_016617.1:g.35977A>T , LRG_788:g.35977A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.1047A>T MANE Select	ENSP00000251810.3:p.Ala349=
ENST00000251810.7:c.1047A>T	ENSP00000251810.3:p.Ala349=
ENST00000395910.6:n.434A>T
ENST00000395912.6:c.891A>T	ENSP00000379248.2:p.Ala297=
ENST00000519317.5:c.411A>T	ENSP00000430641.1:p.Ala137=
ENST00000519962.5:c.192A>T	ENSP00000429140.1:p.Ala64=
ENST00000522368.5:c.1216A>T
ENST00000522394.1:c.380A>T	ENSP00000429578.1:n.380A>T
ENST00000621845.1:c.885A>T	ENSP00000484318.1:p.Ala295=
NM_001172477.1:c.1263A>T , LRG_788t1:c.1263A>T	NP_001165948.1:p.Ala421=
NM_001172478.1:c.891A>T	NP_001165949.1:p.Ala297=
NM_015713.4:c.1047A>T , LRG_788t2:c.1047A>T	NP_056528.2:p.Ala349=
NM_001172478.2:c.891A>T	NP_001165949.1:p.Ala297=
NM_015713.5:c.1047A>T MANE Select	NP_056528.2:p.Ala349=