Canonical Allele Identifier: CA371585841

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220441T>A (hg19) ; chr8:g.102208213T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208213T>A , CM000670.2:g.102208213T>A	GRCh38
NC_000008.10:g.103220441T>A , CM000670.1:g.103220441T>A	GRCh37
NC_000008.9:g.103289617T>A	NCBI36
NG_016617.1:g.35906A>T , LRG_788:g.35906A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.976A>T MANE Select	ENSP00000251810.3:p.Lys326Ter
ENST00000251810.7:c.976A>T	ENSP00000251810.3:p.Lys326Ter
ENST00000395910.6:n.363A>T
ENST00000395912.6:c.820A>T	ENSP00000379248.2:p.Lys274Ter
ENST00000519317.5:c.340A>T	ENSP00000430641.1:p.Lys114Ter
ENST00000519962.5:c.121A>T	ENSP00000429140.1:p.Lys41Ter
ENST00000522368.5:c.1145A>T
ENST00000522394.1:c.309A>T	ENSP00000429578.1:n.309A>T
ENST00000621845.1:c.814A>T	ENSP00000484318.1:p.Lys272Ter
NM_001172477.1:c.1192A>T , LRG_788t1:c.1192A>T	NP_001165948.1:p.Lys398Ter
NM_001172478.1:c.820A>T	NP_001165949.1:p.Lys274Ter
NM_015713.4:c.976A>T , LRG_788t2:c.976A>T	NP_056528.2:p.Lys326Ter
NM_001172478.2:c.820A>T	NP_001165949.1:p.Lys274Ter
NM_015713.5:c.976A>T MANE Select	NP_056528.2:p.Lys326Ter