Canonical Allele Identifier: CA583909881

Gene: RRM2B

Linked Data

• dbSNP Id: rs1348927271
• gnomAD v2: 8-103231188-A-G
• gnomAD v4: 8-102218960-A-G
• MyVariant Identifiers: chr8:g.103231188A>G (hg19) ; chr8:g.102218960A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218960A>G , CM000670.2:g.102218960A>G	GRCh38
NC_000008.10:g.103231188A>G , CM000670.1:g.103231188A>G	GRCh37
NC_000008.9:g.103300364A>G	NCBI36
NG_016617.1:g.25159T>C , LRG_788:g.25159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.551-13T>C MANE Select	ENSP00000251810.3:n.551-13T>C
ENST00000251810.7:c.551-13T>C	ENSP00000251810.3:n.551-13T>C
ENST00000395912.6:c.395-13T>C	ENSP00000379248.2:n.395-13T>C
ENST00000519125.1:n.56T>C
ENST00000519317.5:c.49-4802T>C	ENSP00000430641.1:n.49-4802T>C
ENST00000519962.5:c.49-10675T>C	ENSP00000429140.1:n.49-10675T>C
ENST00000522368.5:c.720-13T>C
ENST00000522394.1:c.123-6071T>C	ENSP00000429578.1:n.123-6071T>C
ENST00000621845.1:c.389-13T>C	ENSP00000484318.1:n.389-13T>C
NM_001172477.1:c.767-13T>C , LRG_788t1:c.767-13T>C	NP_001165948.1:n.767-13T>C
NM_001172478.1:c.395-13T>C	NP_001165949.1:n.395-13T>C
NM_015713.4:c.551-13T>C , LRG_788t2:c.551-13T>C	NP_056528.2:n.551-13T>C
NM_001172478.2:c.395-13T>C	NP_001165949.1:n.395-13T>C
NM_015713.5:c.551-13T>C MANE Select	NP_056528.2:n.551-13T>C