Canonical Allele Identifier: CA182463964
Gene: RRM2B HGNC NCBI

Linked Data

dbSNP Id: rs557867233

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208024G>A , CM000670.2:g.102208024G>A GRCh38
NC_000008.10:g.103220252G>A , CM000670.1:g.103220252G>A GRCh37
NC_000008.9:g.103289428G>A NCBI36
NG_016617.1:g.36095C>T , LRG_788:g.36095C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.*109C>T MANE Select ENSP00000251810.3:n.*109C>T
ENST00000251810.7:c.*109C>T ENSP00000251810.3:n.*109C>T
ENST00000395910.6:n.552C>T
ENST00000522368.5:c.1334C>T
ENST00000621845.1:c.*109C>T ENSP00000484318.1:n.*109C>T
NM_001172477.1:c.*109C>T , LRG_788t1:c.*109C>T NP_001165948.1:n.*109C>T
NM_001172478.1:c.*109C>T NP_001165949.1:n.*109C>T
NM_015713.4:c.*109C>T , LRG_788t2:c.*109C>T NP_056528.2:n.*109C>T
NM_001172478.2:c.*109C>T NP_001165949.1:n.*109C>T
NM_015713.5:c.*109C>T MANE Select NP_056528.2:n.*109C>T