Canonical Allele Identifier: CA2688143442
Gene: RRM2B HGNC NCBI

Linked Data

gnomAD v4: 8-102208121-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208121A>G , CM000670.2:g.102208121A>G GRCh38
NC_000008.10:g.103220349A>G , CM000670.1:g.103220349A>G GRCh37
NC_000008.9:g.103289525A>G NCBI36
NG_016617.1:g.35998T>C , LRG_788:g.35998T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.*12T>C MANE Select ENSP00000251810.3:n.*12T>C
ENST00000251810.7:c.*12T>C ENSP00000251810.3:n.*12T>C
ENST00000395910.6:n.455T>C
ENST00000522368.5:c.1237T>C
ENST00000621845.1:c.*12T>C ENSP00000484318.1:n.*12T>C
NM_001172477.1:c.*12T>C , LRG_788t1:c.*12T>C NP_001165948.1:n.*12T>C
NM_001172478.1:c.*12T>C NP_001165949.1:n.*12T>C
NM_015713.4:c.*12T>C , LRG_788t2:c.*12T>C NP_056528.2:n.*12T>C
NM_001172478.2:c.*12T>C NP_001165949.1:n.*12T>C
NM_015713.5:c.*12T>C MANE Select NP_056528.2:n.*12T>C
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