Canonical Allele Identifier: CA1806678416

Gene: RRM2B

Linked Data

• dbSNP Id: rs1810780566

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218948del , CM000670.2:g.102218948del	GRCh38
NC_000008.10:g.103231176del , CM000670.1:g.103231176del	GRCh37
NC_000008.9:g.103300352del	NCBI36
NG_016617.1:g.25174del , LRG_788:g.25174del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.553del
ENST00000251810.7:c.553del
ENST00000395912.6:c.397del
ENST00000519125.1:n.71del
ENST00000519317.5:c.49-4787del	ENSP00000430641.1:n.49-4787del
ENST00000519962.5:c.49-10660del	ENSP00000429140.1:n.49-10660del
ENST00000522368.5:c.722del
ENST00000522394.1:c.123-6056del	ENSP00000429578.1:n.123-6056del
ENST00000621845.1:c.391del
NM_001172477.1:c.769del , LRG_788t1:c.769del
NM_001172478.1:c.397del
NM_015713.4:c.553del , LRG_788t2:c.553del
NM_001172478.2:c.397del
NM_015713.5:c.553del