Canonical Allele Identifier: CA371585187

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220369C>A (hg19) ; chr8:g.102208141C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208141C>A , CM000670.2:g.102208141C>A	GRCh38
NC_000008.10:g.103220369C>A , CM000670.1:g.103220369C>A	GRCh37
NC_000008.9:g.103289545C>A	NCBI36
NG_016617.1:g.35978G>T , LRG_788:g.35978G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1048G>T MANE Select	ENSP00000251810.3:p.Asp350Tyr
ENST00000251810.7:c.1048G>T	ENSP00000251810.3:p.Asp350Tyr
ENST00000395910.6:n.435G>T
ENST00000395912.6:c.892G>T	ENSP00000379248.2:p.Asp298Tyr
ENST00000519317.5:c.412G>T	ENSP00000430641.1:p.Asp138Tyr
ENST00000519962.5:c.193G>T	ENSP00000429140.1:p.Asp65Tyr
ENST00000522368.5:c.1217G>T
ENST00000522394.1:c.381G>T	ENSP00000429578.1:n.381G>T
ENST00000621845.1:c.886G>T	ENSP00000484318.1:p.Asp296Tyr
NM_001172477.1:c.1264G>T , LRG_788t1:c.1264G>T	NP_001165948.1:p.Asp422Tyr
NM_001172478.1:c.892G>T	NP_001165949.1:p.Asp298Tyr
NM_015713.4:c.1048G>T , LRG_788t2:c.1048G>T	NP_056528.2:p.Asp350Tyr
NM_001172478.2:c.892G>T	NP_001165949.1:p.Asp298Tyr
NM_015713.5:c.1048G>T MANE Select	NP_056528.2:p.Asp350Tyr