Canonical Allele Identifier: CA2089833513
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1950603849
gnomAD v4: 13-48045566-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045566A>G , CM000675.2:g.48045566A>G GRCh38
NC_000013.10:g.48619702A>G , CM000675.1:g.48619702A>G GRCh37
NC_000013.9:g.47517703A>G NCBI36
NG_047021.1:g.13000A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.356-94A>G MANE Select ENSP00000258662.1:n.356-94A>G
ENST00000258662.2:c.356-94A>G ENSP00000258662.1:n.356-94A>G
NM_018283.2:c.356-94A>G NP_060753.1:n.356-94A>G
NM_018283.3:c.356-94A>G NP_060753.1:n.356-94A>G
NR_136687.1:n.536-94A>G
NR_136688.1:n.536-94A>G
NM_018283.4:c.356-94A>G MANE Select NP_060753.1:n.356-94A>G
NR_136687.2:n.377-94A>G
NR_136688.2:n.377-94A>G
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