Canonical Allele Identifier: CA2579221419
Gene: RRM2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102238937T>A , CM000670.2:g.102238937T>A GRCh38
NC_000008.10:g.103251165T>A , CM000670.1:g.103251165T>A GRCh37
NC_000008.9:g.103320341T>A NCBI36
NG_016617.1:g.5182A>T , LRG_788:g.5182A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.-63A>T MANE Select ENSP00000251810.3:n.-63A>T
ENST00000251810.7:c.-63A>T ENSP00000251810.3:n.-63A>T
ENST00000523957.1:c.-63A>T ENSP00000427830.1:n.-63A>T
NM_001172478.1:c.-63A>T NP_001165949.1:n.-63A>T
NM_015713.4:c.-63A>T , LRG_788t2:c.-63A>T NP_056528.2:n.-63A>T
NM_001172478.2:c.-63A>T NP_001165949.1:n.-63A>T
NM_015713.5:c.-63A>T MANE Select NP_056528.2:n.-63A>T