Canonical Allele Identifier: CA388154032
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619797T>A (hg19) chr13:g.48045661T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045661T>A , CM000675.2:g.48045661T>A GRCh38
NC_000013.10:g.48619797T>A , CM000675.1:g.48619797T>A GRCh37
NC_000013.9:g.47517798T>A NCBI36
NG_047021.1:g.13095T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.357T>A MANE Select ENSP00000258662.1:p.Ser119Arg
ENST00000258662.2:c.357T>A ENSP00000258662.1:p.Ser119Arg
NM_018283.2:c.357T>A NP_060753.1:p.Ser119Arg
NM_018283.3:c.357T>A NP_060753.1:p.Ser119Arg
NR_136687.1:n.537T>A
NR_136688.1:n.537T>A
NM_018283.4:c.357T>A MANE Select NP_060753.1:p.Ser119Arg
NR_136687.2:n.378T>A
NR_136688.2:n.378T>A
Search 100 bp 5'
Search 100 bp 3'