Canonical Allele Identifier: CA371586180

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220468A>T (hg19) ; chr8:g.102208240A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208240A>T , CM000670.2:g.102208240A>T	GRCh38
NC_000008.10:g.103220468A>T , CM000670.1:g.103220468A>T	GRCh37
NC_000008.9:g.103289644A>T	NCBI36
NG_016617.1:g.35879T>A , LRG_788:g.35879T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.949T>A MANE Select	ENSP00000251810.3:p.Leu317Ile
ENST00000251810.7:c.949T>A	ENSP00000251810.3:p.Leu317Ile
ENST00000395910.6:n.336T>A
ENST00000395912.6:c.793T>A	ENSP00000379248.2:p.Leu265Ile
ENST00000519317.5:c.313T>A	ENSP00000430641.1:p.Leu105Ile
ENST00000519962.5:c.94T>A	ENSP00000429140.1:p.Leu32Ile
ENST00000522368.5:c.1118T>A
ENST00000522394.1:c.282T>A	ENSP00000429578.1:n.282T>A
ENST00000621845.1:c.787T>A	ENSP00000484318.1:p.Leu263Ile
NM_001172477.1:c.1165T>A , LRG_788t1:c.1165T>A	NP_001165948.1:p.Leu389Ile
NM_001172478.1:c.793T>A	NP_001165949.1:p.Leu265Ile
NM_015713.4:c.949T>A , LRG_788t2:c.949T>A	NP_056528.2:p.Leu317Ile
NM_001172478.2:c.793T>A	NP_001165949.1:p.Leu265Ile
NM_015713.5:c.949T>A MANE Select	NP_056528.2:p.Leu317Ile