Canonical Allele Identifier: CA371596014

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103244418T>G (hg19) ; chr8:g.102232190T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232190T>G , CM000670.2:g.102232190T>G	GRCh38
NC_000008.10:g.103244418T>G , CM000670.1:g.103244418T>G	GRCh37
NC_000008.9:g.103313594T>G	NCBI36
NG_016617.1:g.11929A>C , LRG_788:g.11929A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.163A>C MANE Select	ENSP00000251810.3:p.Met55Leu
ENST00000251810.7:c.163A>C	ENSP00000251810.3:p.Met55Leu
ENST00000395912.6:c.49-6156A>C	ENSP00000379248.2:n.49-6156A>C
ENST00000517517.1:n.472A>C
ENST00000519317.5:c.48+6637A>C	ENSP00000430641.1:n.48+6637A>C
ENST00000519962.5:c.48+6637A>C	ENSP00000429140.1:n.48+6637A>C
ENST00000522368.5:c.332A>C
ENST00000522394.1:c.122+41A>C	ENSP00000429578.1:n.122+41A>C
ENST00000523957.1:c.*86A>C	ENSP00000427830.1:n.*86A>C
ENST00000621845.1:c.1A>C	ENSP00000484318.1:p.Met1Leu
NM_001172477.1:c.379A>C , LRG_788t1:c.379A>C	NP_001165948.1:p.Met127Leu
NM_001172478.1:c.49-6156A>C	NP_001165949.1:n.49-6156A>C
NM_015713.4:c.163A>C , LRG_788t2:c.163A>C	NP_056528.2:p.Met55Leu
NM_001172478.2:c.49-6156A>C	NP_001165949.1:n.49-6156A>C
NM_015713.5:c.163A>C MANE Select	NP_056528.2:p.Met55Leu