Canonical Allele Identifier: CA371591605

Gene: RRM2B

Linked Data

• dbSNP Id: rs863224191
• gnomAD v2: 8-103236304-G-C
• gnomAD v4: 8-102224076-G-C
• MyVariant Identifiers: chr8:g.103236304G>C (hg19) ; chr8:g.102224076G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224076G>C , CM000670.2:g.102224076G>C	GRCh38
NC_000008.10:g.103236304G>C , CM000670.1:g.103236304G>C	GRCh37
NC_000008.9:g.103305480G>C	NCBI36
NG_016617.1:g.20043C>G , LRG_788:g.20043C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.520C>G MANE Select	ENSP00000251810.3:p.Arg174Gly
ENST00000251810.7:c.520C>G	ENSP00000251810.3:p.Arg174Gly
ENST00000395912.6:c.364C>G	ENSP00000379248.2:p.Arg122Gly
ENST00000519317.5:c.49-9918C>G	ENSP00000430641.1:n.49-9918C>G
ENST00000519962.5:c.48+14751C>G	ENSP00000429140.1:n.48+14751C>G
ENST00000522368.5:c.689C>G
ENST00000522394.1:c.122+8155C>G	ENSP00000429578.1:n.122+8155C>G
ENST00000621845.1:c.358C>G	ENSP00000484318.1:p.Arg120Gly
NM_001172477.1:c.736C>G , LRG_788t1:c.736C>G	NP_001165948.1:p.Arg246Gly
NM_001172478.1:c.364C>G	NP_001165949.1:p.Arg122Gly
NM_015713.4:c.520C>G , LRG_788t2:c.520C>G	NP_056528.2:p.Arg174Gly
NM_001172478.2:c.364C>G	NP_001165949.1:p.Arg122Gly
NM_015713.5:c.520C>G MANE Select	NP_056528.2:p.Arg174Gly