Canonical Allele Identifier: CA844764485

Gene: RRM2B

Linked Data

• dbSNP Id: rs1347324619
• gnomAD v4: 8-102208057-A-T
• MyVariant Identifiers: chr8:g.103220285A>T (hg19) ; chr8:g.102208057A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208057A>T , CM000670.2:g.102208057A>T	GRCh38
NC_000008.10:g.103220285A>T , CM000670.1:g.103220285A>T	GRCh37
NC_000008.9:g.103289461A>T	NCBI36
NG_016617.1:g.36062T>A , LRG_788:g.36062T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*76T>A MANE Select	ENSP00000251810.3:n.*76T>A
ENST00000251810.7:c.*76T>A	ENSP00000251810.3:n.*76T>A
ENST00000395910.6:n.519T>A
ENST00000522368.5:c.1301T>A
ENST00000621845.1:c.*76T>A	ENSP00000484318.1:n.*76T>A
NM_001172477.1:c.*76T>A , LRG_788t1:c.*76T>A	NP_001165948.1:n.*76T>A
NM_001172478.1:c.*76T>A	NP_001165949.1:n.*76T>A
NM_015713.4:c.*76T>A , LRG_788t2:c.*76T>A	NP_056528.2:n.*76T>A
NM_001172478.2:c.*76T>A	NP_001165949.1:n.*76T>A
NM_015713.5:c.*76T>A MANE Select	NP_056528.2:n.*76T>A