Canonical Allele Identifier: CA371585903

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102208216-C-A
• MyVariant Identifiers: chr8:g.103220444C>A (hg19) ; chr8:g.102208216C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208216C>A , CM000670.2:g.102208216C>A	GRCh38
NC_000008.10:g.103220444C>A , CM000670.1:g.103220444C>A	GRCh37
NC_000008.9:g.103289620C>A	NCBI36
NG_016617.1:g.35903G>T , LRG_788:g.35903G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.973G>T MANE Select	ENSP00000251810.3:p.Glu325Ter
ENST00000251810.7:c.973G>T	ENSP00000251810.3:p.Glu325Ter
ENST00000395910.6:n.360G>T
ENST00000395912.6:c.817G>T	ENSP00000379248.2:p.Glu273Ter
ENST00000519317.5:c.337G>T	ENSP00000430641.1:p.Glu113Ter
ENST00000519962.5:c.118G>T	ENSP00000429140.1:p.Glu40Ter
ENST00000522368.5:c.1142G>T
ENST00000522394.1:c.306G>T	ENSP00000429578.1:n.306G>T
ENST00000621845.1:c.811G>T	ENSP00000484318.1:p.Glu271Ter
NM_001172477.1:c.1189G>T , LRG_788t1:c.1189G>T	NP_001165948.1:p.Glu397Ter
NM_001172478.1:c.817G>T	NP_001165949.1:p.Glu273Ter
NM_015713.4:c.973G>T , LRG_788t2:c.973G>T	NP_056528.2:p.Glu325Ter
NM_001172478.2:c.817G>T	NP_001165949.1:p.Glu273Ter
NM_015713.5:c.973G>T MANE Select	NP_056528.2:p.Glu325Ter