Canonical Allele Identifier: CA371585925

Gene: RRM2B

Linked Data

• dbSNP Id: rs1343432124
• gnomAD v2: 8-103220446-A-G
• gnomAD v4: 8-102208218-A-G
• MyVariant Identifiers: chr8:g.103220446A>G (hg19) ; chr8:g.102208218A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208218A>G , CM000670.2:g.102208218A>G	GRCh38
NC_000008.10:g.103220446A>G , CM000670.1:g.103220446A>G	GRCh37
NC_000008.9:g.103289622A>G	NCBI36
NG_016617.1:g.35901T>C , LRG_788:g.35901T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.971T>C MANE Select	ENSP00000251810.3:p.Phe324Ser
ENST00000251810.7:c.971T>C	ENSP00000251810.3:p.Phe324Ser
ENST00000395910.6:n.358T>C
ENST00000395912.6:c.815T>C	ENSP00000379248.2:p.Phe272Ser
ENST00000519317.5:c.335T>C	ENSP00000430641.1:p.Phe112Ser
ENST00000519962.5:c.116T>C	ENSP00000429140.1:p.Phe39Ser
ENST00000522368.5:c.1140T>C
ENST00000522394.1:c.304T>C	ENSP00000429578.1:n.304T>C
ENST00000621845.1:c.809T>C	ENSP00000484318.1:p.Phe270Ser
NM_001172477.1:c.1187T>C , LRG_788t1:c.1187T>C	NP_001165948.1:p.Phe396Ser
NM_001172478.1:c.815T>C	NP_001165949.1:p.Phe272Ser
NM_015713.4:c.971T>C , LRG_788t2:c.971T>C	NP_056528.2:p.Phe324Ser
NM_001172478.2:c.815T>C	NP_001165949.1:p.Phe272Ser
NM_015713.5:c.971T>C MANE Select	NP_056528.2:p.Phe324Ser