Canonical Allele Identifier: CA371585181

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220366A>G (hg19) ; chr8:g.102208138A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208138A>G , CM000670.2:g.102208138A>G	GRCh38
NC_000008.10:g.103220366A>G , CM000670.1:g.103220366A>G	GRCh37
NC_000008.9:g.103289542A>G	NCBI36
NG_016617.1:g.35981T>C , LRG_788:g.35981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1051T>C MANE Select	ENSP00000251810.3:p.Phe351Leu
ENST00000251810.7:c.1051T>C	ENSP00000251810.3:p.Phe351Leu
ENST00000395910.6:n.438T>C
ENST00000395912.6:c.895T>C	ENSP00000379248.2:p.Phe299Leu
ENST00000519317.5:c.415T>C	ENSP00000430641.1:p.Phe139Leu
ENST00000519962.5:c.196T>C	ENSP00000429140.1:p.Phe66Leu
ENST00000522368.5:c.1220T>C
ENST00000522394.1:c.384T>C	ENSP00000429578.1:n.384T>C
ENST00000621845.1:c.889T>C	ENSP00000484318.1:p.Phe297Leu
NM_001172477.1:c.1267T>C , LRG_788t1:c.1267T>C	NP_001165948.1:p.Phe423Leu
NM_001172478.1:c.895T>C	NP_001165949.1:p.Phe299Leu
NM_015713.4:c.1051T>C , LRG_788t2:c.1051T>C	NP_056528.2:p.Phe351Leu
NM_001172478.2:c.895T>C	NP_001165949.1:p.Phe299Leu
NM_015713.5:c.1051T>C MANE Select	NP_056528.2:p.Phe351Leu