Canonical Allele Identifier: CA371590521

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103231170T>A (hg19) ; chr8:g.102218942T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218942T>A , CM000670.2:g.102218942T>A	GRCh38
NC_000008.10:g.103231170T>A , CM000670.1:g.103231170T>A	GRCh37
NC_000008.9:g.103300346T>A	NCBI36
NG_016617.1:g.25177A>T , LRG_788:g.25177A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.556A>T MANE Select	ENSP00000251810.3:p.Arg186Ter
ENST00000251810.7:c.556A>T	ENSP00000251810.3:p.Arg186Ter
ENST00000395912.6:c.400A>T	ENSP00000379248.2:p.Arg134Ter
ENST00000519125.1:n.74A>T
ENST00000519317.5:c.49-4784A>T	ENSP00000430641.1:n.49-4784A>T
ENST00000519962.5:c.49-10657A>T	ENSP00000429140.1:n.49-10657A>T
ENST00000522368.5:c.725A>T
ENST00000522394.1:c.123-6053A>T	ENSP00000429578.1:n.123-6053A>T
ENST00000621845.1:c.394A>T	ENSP00000484318.1:p.Arg132Ter
NM_001172477.1:c.772A>T , LRG_788t1:c.772A>T	NP_001165948.1:p.Arg258Ter
NM_001172478.1:c.400A>T	NP_001165949.1:p.Arg134Ter
NM_015713.4:c.556A>T , LRG_788t2:c.556A>T	NP_056528.2:p.Arg186Ter
NM_001172478.2:c.400A>T	NP_001165949.1:p.Arg134Ter
NM_015713.5:c.556A>T MANE Select	NP_056528.2:p.Arg186Ter