Canonical Allele Identifier: CA388154056
Gene: NUDT15 HGNC NCBI

Linked Data

gnomAD v4: 13-48045664-G-C
MyVariant Identifiers: chr13:g.48619800G>C (hg19) chr13:g.48045664G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045664G>C , CM000675.2:g.48045664G>C GRCh38
NC_000013.10:g.48619800G>C , CM000675.1:g.48619800G>C GRCh37
NC_000013.9:g.47517801G>C NCBI36
NG_047021.1:g.13098G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.360G>C MANE Select ENSP00000258662.1:p.Trp120Cys
ENST00000258662.2:c.360G>C ENSP00000258662.1:p.Trp120Cys
NM_018283.2:c.360G>C NP_060753.1:p.Trp120Cys
NM_018283.3:c.360G>C NP_060753.1:p.Trp120Cys
NR_136687.1:n.540G>C
NR_136688.1:n.540G>C
NM_018283.4:c.360G>C MANE Select NP_060753.1:p.Trp120Cys
NR_136687.2:n.381G>C
NR_136688.2:n.381G>C
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