Canonical Allele Identifier: CA371588241

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102212891T>C , CM000670.2:g.102212891T>C	GRCh38
NC_000008.10:g.103225119T>C , CM000670.1:g.103225119T>C	GRCh37
NC_000008.9:g.103294295T>C	NCBI36
NG_016617.1:g.31228A>G , LRG_788:g.31228A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.790-2A>G MANE Select	NP_056528.2:n.790-2A>G
ENST00000251810.8:c.790-2A>G MANE Select	ENSP00000251810.3:n.790-2A>G
NM_001172477.1:c.1006-2A>G , LRG_788t1:c.1006-2A>G	NP_001165948.1:n.1006-2A>G
NM_001172478.1:c.634-2A>G	NP_001165949.1:n.634-2A>G
NM_001172478.2:c.634-2A>G	NP_001165949.1:n.634-2A>G
NM_015713.4:c.790-2A>G , LRG_788t2:c.790-2A>G	NP_056528.2:n.790-2A>G
ENST00000251810.7:c.790-2A>G	ENSP00000251810.3:n.790-2A>G
ENST00000395910.6:n.177-2A>G
ENST00000395912.6:c.634-2A>G	ENSP00000379248.2:n.634-2A>G
ENST00000519125.1:n.308-2A>G
ENST00000519317.5:c.154-2A>G	ENSP00000430641.1:n.154-2A>G
ENST00000519962.5:c.49-4606A>G	ENSP00000429140.1:n.49-4606A>G
ENST00000522368.5:c.959-2A>G
ENST00000522394.1:c.123-2A>G	ENSP00000429578.1:n.123-2A>G
ENST00000621845.1:c.628-2A>G	ENSP00000484318.1:n.628-2A>G