Canonical Allele Identifier: CA462127635

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237121G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224893G>T , CM000670.2:g.102224893G>T	GRCh38
NC_000008.10:g.103237121G>T , CM000670.1:g.103237121G>T	GRCh37
NC_000008.9:g.103306297G>T	NCBI36
NG_016617.1:g.19226C>A , LRG_788:g.19226C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.447C>A MANE Select	ENSP00000251810.3:p.Pro149=
ENST00000251810.7:c.447C>A	ENSP00000251810.3:p.Pro149=
ENST00000395912.6:c.291C>A	ENSP00000379248.2:p.Pro97=
ENST00000519317.5:c.49-10735C>A	ENSP00000430641.1:n.49-10735C>A
ENST00000519962.5:c.48+13934C>A	ENSP00000429140.1:n.48+13934C>A
ENST00000522368.5:c.616C>A
ENST00000522394.1:c.122+7338C>A	ENSP00000429578.1:n.122+7338C>A
ENST00000621845.1:c.285C>A	ENSP00000484318.1:p.Pro95=
NM_001172477.1:c.663C>A , LRG_788t1:c.663C>A	NP_001165948.1:p.Pro221=
NM_001172478.1:c.291C>A	NP_001165949.1:p.Pro97=
NM_015713.4:c.447C>A , LRG_788t2:c.447C>A	NP_056528.2:p.Pro149=
NM_001172478.2:c.291C>A	NP_001165949.1:p.Pro97=
NM_015713.5:c.447C>A MANE Select	NP_056528.2:p.Pro149=