Canonical Allele Identifier: CA182464137

Gene: RRM2B

Linked Data

• dbSNP Id: rs1265117
• gnomAD v3: 8-102208123-G-A
• gnomAD v4: 8-102208123-G-A
• MyVariant Identifiers: chr8:g.102208123G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208123G>A , CM000670.2:g.102208123G>A	GRCh38
NG_016617.1:g.35996C>T , LRG_788:g.35996C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.*10C>T MANE Select	ENSP00000251810.3:n.*10C>T
ENST00000251810.7:c.*10C>T	ENSP00000251810.3:n.*10C>T
ENST00000395910.6:n.453C>T
ENST00000522368.5:c.1235C>T
ENST00000621845.1:c.*10C>T	ENSP00000484318.1:n.*10C>T
NM_001172477.1:c.*10C>T , LRG_788t1:c.*10C>T	NP_001165948.1:n.*10C>T
NM_001172478.1:c.*10C>T	NP_001165949.1:n.*10C>T
NM_015713.4:c.*10C>T , LRG_788t2:c.*10C>T	NP_056528.2:n.*10C>T
NM_001172478.2:c.*10C>T	NP_001165949.1:n.*10C>T
NM_015713.5:c.*10C>T MANE Select	NP_056528.2:n.*10C>T