Canonical Allele Identifier: CA371585274

Gene: RRM2B

Linked Data

• dbSNP Id: rs376690511
• gnomAD v3: 8-102208160-G-T
• gnomAD v4: 8-102208160-G-T
• MyVariant Identifiers: chr8:g.103220388G>T (hg19) ; chr8:g.102208160G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208160G>T , CM000670.2:g.102208160G>T	GRCh38
NC_000008.10:g.103220388G>T , CM000670.1:g.103220388G>T	GRCh37
NC_000008.9:g.103289564G>T	NCBI36
NG_016617.1:g.35959C>A , LRG_788:g.35959C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1029C>A MANE Select	ENSP00000251810.3:p.Asn343Lys
ENST00000251810.7:c.1029C>A	ENSP00000251810.3:p.Asn343Lys
ENST00000395910.6:n.416C>A
ENST00000395912.6:c.873C>A	ENSP00000379248.2:p.Asn291Lys
ENST00000519317.5:c.393C>A	ENSP00000430641.1:p.Asn131Lys
ENST00000519962.5:c.174C>A	ENSP00000429140.1:p.Asn58Lys
ENST00000522368.5:c.1198C>A
ENST00000522394.1:c.362C>A	ENSP00000429578.1:n.362C>A
ENST00000621845.1:c.867C>A	ENSP00000484318.1:p.Asn289Lys
NM_001172477.1:c.1245C>A , LRG_788t1:c.1245C>A	NP_001165948.1:p.Asn415Lys
NM_001172478.1:c.873C>A	NP_001165949.1:p.Asn291Lys
NM_015713.4:c.1029C>A , LRG_788t2:c.1029C>A	NP_056528.2:p.Asn343Lys
NM_001172478.2:c.873C>A	NP_001165949.1:p.Asn291Lys
NM_015713.5:c.1029C>A MANE Select	NP_056528.2:p.Asn343Lys