Canonical Allele Identifier: CA462127231

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103231174C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218946C>A , CM000670.2:g.102218946C>A	GRCh38
NC_000008.10:g.103231174C>A , CM000670.1:g.103231174C>A	GRCh37
NC_000008.9:g.103300350C>A	NCBI36
NG_016617.1:g.25173G>T , LRG_788:g.25173G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.552G>T MANE Select	ENSP00000251810.3:p.Gly184=
ENST00000251810.7:c.552G>T	ENSP00000251810.3:p.Gly184=
ENST00000395912.6:c.396G>T	ENSP00000379248.2:p.Gly132=
ENST00000519125.1:n.70G>T
ENST00000519317.5:c.49-4788G>T	ENSP00000430641.1:n.49-4788G>T
ENST00000519962.5:c.49-10661G>T	ENSP00000429140.1:n.49-10661G>T
ENST00000522368.5:c.721G>T
ENST00000522394.1:c.123-6057G>T	ENSP00000429578.1:n.123-6057G>T
ENST00000621845.1:c.390G>T	ENSP00000484318.1:p.Gly130=
NM_001172477.1:c.768G>T , LRG_788t1:c.768G>T	NP_001165948.1:p.Gly256=
NM_001172478.1:c.396G>T	NP_001165949.1:p.Gly132=
NM_015713.4:c.552G>T , LRG_788t2:c.552G>T	NP_056528.2:p.Gly184=
NM_001172478.2:c.396G>T	NP_001165949.1:p.Gly132=
NM_015713.5:c.552G>T MANE Select	NP_056528.2:p.Gly184=