Canonical Allele Identifier: CA249274272
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs541689297
gnomAD v3: 13-48046017-A-G
gnomAD v4: 13-48046017-A-G
MyVariant Identifiers: chr13:g.48620153A>G (hg19) chr13:g.48046017A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48046017A>G , CM000675.2:g.48046017A>G GRCh38
NC_000013.10:g.48620153A>G , CM000675.1:g.48620153A>G GRCh37
NC_000013.9:g.47518154A>G NCBI36
NG_047021.1:g.13451A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*218A>G MANE Select ENSP00000258662.1:n.*218A>G
ENST00000258662.2:c.*218A>G ENSP00000258662.1:n.*218A>G
NM_018283.2:c.*218A>G NP_060753.1:n.*218A>G
NM_018283.3:c.*218A>G NP_060753.1:n.*218A>G
NR_136687.1:n.718+175A>G
NR_136688.1:n.675+218A>G
NM_018283.4:c.*218A>G MANE Select NP_060753.1:n.*218A>G
NR_136687.2:n.559+175A>G
NR_136688.2:n.516+218A>G
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