Canonical Allele Identifier: CA1630834292
Gene: RRM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10122793T= , CM000664.2:g.10122793T= GRCh38
NC_000002.11:g.10262920T= , CM000664.1:g.10262920T= GRCh37
NC_000002.10:g.10180371T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304567.10:c.-6T= MANE Select ENSP00000302955.4:n.-6T=
ENST00000641198.1:c.-6T= ENSP00000493399.1:n.-6T=
ENST00000641498.1:c.-6T= ENSP00000493425.1:n.-6T=
ENST00000652660.1:n.64T=
ENST00000304567.9:c.-6T= ENSP00000302955.4:n.-6T=
ENST00000360566.6:c.175T= ENSP00000353770.2:p.Ser59=
ENST00000459969.5:n.82T=
ENST00000461327.5:n.55T=
ENST00000491447.1:n.42T=
ENST00000498343.5:n.55T=
ENST00000615152.4:c.175T= ENSP00000484183.1:p.Ser59=
NM_001034.3:c.-6T= NP_001025.1:n.-6T=
NM_001165931.1:c.175T= NP_001159403.1:p.Ser59=
NM_001034.4:c.-6T= MANE Select NP_001025.1:n.-6T=
NR_164157.1:n.55T=