Canonical Allele Identifier: CA4830954
Gene: RRM2B HGNC NCBI

Linked Data

dbSNP Id: rs1265117
gnomAD v4: 8-102208123-G-T
MyVariant Identifiers: chr8:g.102208123G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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