Canonical Allele Identifier: CA1806678429

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218951G= , CM000670.2:g.102218951G=	GRCh38
NC_000008.10:g.103231179G= , CM000670.1:g.103231179G=	GRCh37
NC_000008.9:g.103300355G=	NCBI36
NG_016617.1:g.25168C= , LRG_788:g.25168C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.551-4C= MANE Select	ENSP00000251810.3:n.551-4C=
ENST00000251810.7:c.551-4C=	ENSP00000251810.3:n.551-4C=
ENST00000395912.6:c.395-4C=	ENSP00000379248.2:n.395-4C=
ENST00000519125.1:n.65C=
ENST00000519317.5:c.49-4793C=	ENSP00000430641.1:n.49-4793C=
ENST00000519962.5:c.49-10666C=	ENSP00000429140.1:n.49-10666C=
ENST00000522368.5:c.720-4C=
ENST00000522394.1:c.123-6062C=	ENSP00000429578.1:n.123-6062C=
ENST00000621845.1:c.389-4C=	ENSP00000484318.1:n.389-4C=
NM_001172477.1:c.767-4C= , LRG_788t1:c.767-4C=	NP_001165948.1:n.767-4C=
NM_001172478.1:c.395-4C=	NP_001165949.1:n.395-4C=
NM_015713.4:c.551-4C= , LRG_788t2:c.551-4C=	NP_056528.2:n.551-4C=
NM_001172478.2:c.395-4C=	NP_001165949.1:n.395-4C=
NM_015713.5:c.551-4C= MANE Select	NP_056528.2:n.551-4C=