Canonical Allele Identifier: CA371586129
Gene: RRM2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208234C>G , CM000670.2:g.102208234C>G GRCh38
NC_000008.10:g.103220462C>G , CM000670.1:g.103220462C>G GRCh37
NC_000008.9:g.103289638C>G NCBI36
NG_016617.1:g.35885G>C , LRG_788:g.35885G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.955G>C MANE Select ENSP00000251810.3:p.Gly319Arg
ENST00000251810.7:c.955G>C ENSP00000251810.3:p.Gly319Arg
ENST00000395910.6:n.342G>C
ENST00000395912.6:c.799G>C ENSP00000379248.2:p.Gly267Arg
ENST00000519317.5:c.319G>C ENSP00000430641.1:p.Gly107Arg
ENST00000519962.5:c.100G>C ENSP00000429140.1:p.Gly34Arg
ENST00000522368.5:c.1124G>C
ENST00000522394.1:c.288G>C ENSP00000429578.1:n.288G>C
ENST00000621845.1:c.793G>C ENSP00000484318.1:p.Gly265Arg
NM_001172477.1:c.1171G>C , LRG_788t1:c.1171G>C NP_001165948.1:p.Gly391Arg
NM_001172478.1:c.799G>C NP_001165949.1:p.Gly267Arg
NM_015713.4:c.955G>C , LRG_788t2:c.955G>C NP_056528.2:p.Gly319Arg
NM_001172478.2:c.799G>C NP_001165949.1:p.Gly267Arg
NM_015713.5:c.955G>C MANE Select NP_056528.2:p.Gly319Arg