Canonical Allele Identifier: CA371590539

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103231175C>G (hg19) ; chr8:g.102218947C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218947C>G , CM000670.2:g.102218947C>G	GRCh38
NC_000008.10:g.103231175C>G , CM000670.1:g.103231175C>G	GRCh37
NC_000008.9:g.103300351C>G	NCBI36
NG_016617.1:g.25172G>C , LRG_788:g.25172G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.551G>C MANE Select	ENSP00000251810.3:p.Gly184Ala
ENST00000251810.7:c.551G>C	ENSP00000251810.3:p.Gly184Ala
ENST00000395912.6:c.395G>C	ENSP00000379248.2:p.Gly132Ala
ENST00000519125.1:n.69G>C
ENST00000519317.5:c.49-4789G>C	ENSP00000430641.1:n.49-4789G>C
ENST00000519962.5:c.49-10662G>C	ENSP00000429140.1:n.49-10662G>C
ENST00000522368.5:c.720G>C
ENST00000522394.1:c.123-6058G>C	ENSP00000429578.1:n.123-6058G>C
ENST00000621845.1:c.389G>C	ENSP00000484318.1:p.Gly130Ala
NM_001172477.1:c.767G>C , LRG_788t1:c.767G>C	NP_001165948.1:p.Gly256Ala
NM_001172478.1:c.395G>C	NP_001165949.1:p.Gly132Ala
NM_015713.4:c.551G>C , LRG_788t2:c.551G>C	NP_056528.2:p.Gly184Ala
NM_001172478.2:c.395G>C	NP_001165949.1:p.Gly132Ala
NM_015713.5:c.551G>C MANE Select	NP_056528.2:p.Gly184Ala