Canonical Allele Identifier: CA698626565
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1039497122
gnomAD v3: 13-48045931-C-T
gnomAD v4: 13-48045931-C-T
MyVariant Identifiers: chr13:g.48620067C>T (hg19) chr13:g.48045931C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045931C>T , CM000675.2:g.48045931C>T GRCh38
NC_000013.10:g.48620067C>T , CM000675.1:g.48620067C>T GRCh37
NC_000013.9:g.47518068C>T NCBI36
NG_047021.1:g.13365C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*132C>T MANE Select ENSP00000258662.1:n.*132C>T
ENST00000258662.2:c.*132C>T ENSP00000258662.1:n.*132C>T
NM_018283.2:c.*132C>T NP_060753.1:n.*132C>T
NM_018283.3:c.*132C>T NP_060753.1:n.*132C>T
NR_136687.1:n.718+89C>T
NR_136688.1:n.675+132C>T
NM_018283.4:c.*132C>T MANE Select NP_060753.1:n.*132C>T
NR_136687.2:n.559+89C>T
NR_136688.2:n.516+132C>T
Search 100 bp 5'
Search 100 bp 3'