Canonical Allele Identifier: CA2688144935
Gene: RRM2B HGNC NCBI

Linked Data

gnomAD v4: 8-102238948-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102238948C>A , CM000670.2:g.102238948C>A GRCh38
NC_000008.10:g.103251176C>A , CM000670.1:g.103251176C>A GRCh37
NC_000008.9:g.103320352C>A NCBI36
NG_016617.1:g.5171G>T , LRG_788:g.5171G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.-74G>T MANE Select ENSP00000251810.3:n.-74G>T
ENST00000251810.7:c.-74G>T ENSP00000251810.3:n.-74G>T
NM_001172478.1:c.-74G>T NP_001165949.1:n.-74G>T
NM_015713.4:c.-74G>T , LRG_788t2:c.-74G>T NP_056528.2:n.-74G>T
NM_001172478.2:c.-74G>T NP_001165949.1:n.-74G>T
NM_015713.5:c.-74G>T MANE Select NP_056528.2:n.-74G>T
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