Canonical Allele Identifier: CA2688143402
Gene: RRM2B HGNC NCBI

Linked Data

gnomAD v4: 8-102208031-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.102208031C>T , CM000670.2:g.102208031C>T GRCh38
NC_000008.10:g.103220259C>T , CM000670.1:g.103220259C>T GRCh37
NC_000008.9:g.103289435C>T NCBI36
NG_016617.1:g.36088G>A , LRG_788:g.36088G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251810.8:c.*102G>A MANE Select ENSP00000251810.3:n.*102G>A
ENST00000251810.7:c.*102G>A ENSP00000251810.3:n.*102G>A
ENST00000395910.6:n.545G>A
ENST00000522368.5:c.1327G>A
ENST00000621845.1:c.*102G>A ENSP00000484318.1:n.*102G>A
NM_001172477.1:c.*102G>A , LRG_788t1:c.*102G>A NP_001165948.1:n.*102G>A
NM_001172478.1:c.*102G>A NP_001165949.1:n.*102G>A
NM_015713.4:c.*102G>A , LRG_788t2:c.*102G>A NP_056528.2:n.*102G>A
NM_001172478.2:c.*102G>A NP_001165949.1:n.*102G>A
NM_015713.5:c.*102G>A MANE Select NP_056528.2:n.*102G>A
Search 100 bp 5'
Search 100 bp 3'