Canonical Allele Identifier: CA2579221328

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102225107-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102225107T>A , CM000670.2:g.102225107T>A	GRCh38
NC_000008.10:g.103237335T>A , CM000670.1:g.103237335T>A	GRCh37
NC_000008.9:g.103306511T>A	NCBI36
NG_016617.1:g.19012A>T , LRG_788:g.19012A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.322-89A>T MANE Select	ENSP00000251810.3:n.322-89A>T
ENST00000251810.7:c.322-89A>T	ENSP00000251810.3:n.322-89A>T
ENST00000395912.6:c.166-89A>T	ENSP00000379248.2:n.166-89A>T
ENST00000519317.5:c.49-10949A>T	ENSP00000430641.1:n.49-10949A>T
ENST00000519962.5:c.48+13720A>T	ENSP00000429140.1:n.48+13720A>T
ENST00000522368.5:c.491-89A>T
ENST00000522394.1:c.122+7124A>T	ENSP00000429578.1:n.122+7124A>T
ENST00000523957.1:c.*245-89A>T	ENSP00000427830.1:n.*245-89A>T
ENST00000621845.1:c.160-89A>T	ENSP00000484318.1:n.160-89A>T
NM_001172477.1:c.538-89A>T , LRG_788t1:c.538-89A>T	NP_001165948.1:n.538-89A>T
NM_001172478.1:c.166-89A>T	NP_001165949.1:n.166-89A>T
NM_015713.4:c.322-89A>T , LRG_788t2:c.322-89A>T	NP_056528.2:n.322-89A>T
NM_001172478.2:c.166-89A>T	NP_001165949.1:n.166-89A>T
NM_015713.5:c.322-89A>T MANE Select	NP_056528.2:n.322-89A>T