Canonical Allele Identifier: CA1806678434

Gene: RRM2B

Linked Data

• dbSNP Id: rs1810780789
• gnomAD v4: 8-102218956-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218956C>T , CM000670.2:g.102218956C>T	GRCh38
NC_000008.10:g.103231184C>T , CM000670.1:g.103231184C>T	GRCh37
NC_000008.9:g.103300360C>T	NCBI36
NG_016617.1:g.25163G>A , LRG_788:g.25163G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.551-9G>A MANE Select	ENSP00000251810.3:n.551-9G>A
ENST00000251810.7:c.551-9G>A	ENSP00000251810.3:n.551-9G>A
ENST00000395912.6:c.395-9G>A	ENSP00000379248.2:n.395-9G>A
ENST00000519125.1:n.60G>A
ENST00000519317.5:c.49-4798G>A	ENSP00000430641.1:n.49-4798G>A
ENST00000519962.5:c.49-10671G>A	ENSP00000429140.1:n.49-10671G>A
ENST00000522368.5:c.720-9G>A
ENST00000522394.1:c.123-6067G>A	ENSP00000429578.1:n.123-6067G>A
ENST00000621845.1:c.389-9G>A	ENSP00000484318.1:n.389-9G>A
NM_001172477.1:c.767-9G>A , LRG_788t1:c.767-9G>A	NP_001165948.1:n.767-9G>A
NM_001172478.1:c.395-9G>A	NP_001165949.1:n.395-9G>A
NM_015713.4:c.551-9G>A , LRG_788t2:c.551-9G>A	NP_056528.2:n.551-9G>A
NM_001172478.2:c.395-9G>A	NP_001165949.1:n.395-9G>A
NM_015713.5:c.551-9G>A MANE Select	NP_056528.2:n.551-9G>A