Canonical Allele Identifier: CA955771589
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1950606921
gnomAD v3: 13-48045974-T-G
gnomAD v4: 13-48045974-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045974T>G , CM000675.2:g.48045974T>G GRCh38
NC_000013.10:g.48620110T>G , CM000675.1:g.48620110T>G GRCh37
NC_000013.9:g.47518111T>G NCBI36
NG_047021.1:g.13408T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*175T>G MANE Select ENSP00000258662.1:n.*175T>G
ENST00000258662.2:c.*175T>G ENSP00000258662.1:n.*175T>G
NM_018283.2:c.*175T>G NP_060753.1:n.*175T>G
NM_018283.3:c.*175T>G NP_060753.1:n.*175T>G
NR_136687.1:n.718+132T>G
NR_136688.1:n.675+175T>G
NM_018283.4:c.*175T>G MANE Select NP_060753.1:n.*175T>G
NR_136687.2:n.559+132T>G
NR_136688.2:n.516+175T>G
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