Canonical Allele Identifier: CA1806674658
Gene: RRM2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208127G= , CM000670.2:g.102208127G= GRCh38
NC_000008.10:g.103220355G= , CM000670.1:g.103220355G= GRCh37
NC_000008.9:g.103289531G= NCBI36
NG_016617.1:g.35992C= , LRG_788:g.35992C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.*6C= MANE Select ENSP00000251810.3:n.*6C=
ENST00000251810.7:c.*6C= ENSP00000251810.3:n.*6C=
ENST00000395910.6:n.449C=
ENST00000522368.5:c.1231C=
ENST00000621845.1:c.*6C= ENSP00000484318.1:n.*6C=
NM_001172477.1:c.*6C= , LRG_788t1:c.*6C= NP_001165948.1:n.*6C=
NM_001172478.1:c.*6C= NP_001165949.1:n.*6C=
NM_015713.4:c.*6C= , LRG_788t2:c.*6C= NP_056528.2:n.*6C=
NM_001172478.2:c.*6C= NP_001165949.1:n.*6C=
NM_015713.5:c.*6C= MANE Select NP_056528.2:n.*6C=