Canonical Allele Identifier: CA371586022

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220452T>A (hg19) ; chr8:g.102208224T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208224T>A , CM000670.2:g.102208224T>A	GRCh38
NC_000008.10:g.103220452T>A , CM000670.1:g.103220452T>A	GRCh37
NC_000008.9:g.103289628T>A	NCBI36
NG_016617.1:g.35895A>T , LRG_788:g.35895A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.965A>T MANE Select	ENSP00000251810.3:p.Asn322Ile
ENST00000251810.7:c.965A>T	ENSP00000251810.3:p.Asn322Ile
ENST00000395910.6:n.352A>T
ENST00000395912.6:c.809A>T	ENSP00000379248.2:p.Asn270Ile
ENST00000519317.5:c.329A>T	ENSP00000430641.1:p.Asn110Ile
ENST00000519962.5:c.110A>T	ENSP00000429140.1:p.Asn37Ile
ENST00000522368.5:c.1134A>T
ENST00000522394.1:c.298A>T	ENSP00000429578.1:n.298A>T
ENST00000621845.1:c.803A>T	ENSP00000484318.1:p.Asn268Ile
NM_001172477.1:c.1181A>T , LRG_788t1:c.1181A>T	NP_001165948.1:p.Asn394Ile
NM_001172478.1:c.809A>T	NP_001165949.1:p.Asn270Ile
NM_015713.4:c.965A>T , LRG_788t2:c.965A>T	NP_056528.2:p.Asn322Ile
NM_001172478.2:c.809A>T	NP_001165949.1:p.Asn270Ile
NM_015713.5:c.965A>T MANE Select	NP_056528.2:p.Asn322Ile