Canonical Allele Identifier: CA2688144920
Gene: RRM2B HGNC NCBI

Linked Data

gnomAD v4: 8-102238927-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102238927C>T , CM000670.2:g.102238927C>T GRCh38
NC_000008.10:g.103251155C>T , CM000670.1:g.103251155C>T GRCh37
NC_000008.9:g.103320331C>T NCBI36
NG_016617.1:g.5192G>A , LRG_788:g.5192G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251810.8:c.-53G>A MANE Select ENSP00000251810.3:n.-53G>A
ENST00000251810.7:c.-53G>A ENSP00000251810.3:n.-53G>A
ENST00000523957.1:c.-53G>A ENSP00000427830.1:n.-53G>A
NM_001172478.1:c.-53G>A NP_001165949.1:n.-53G>A
NM_015713.4:c.-53G>A , LRG_788t2:c.-53G>A NP_056528.2:n.-53G>A
NM_001172478.2:c.-53G>A NP_001165949.1:n.-53G>A
NM_015713.5:c.-53G>A MANE Select NP_056528.2:n.-53G>A
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