Canonical Allele Identifier: CA698626174
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1321338453
gnomAD v3: 13-48045586-G-A
gnomAD v4: 13-48045586-G-A
MyVariant Identifiers: chr13:g.48619722G>A (hg19) chr13:g.48045586G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045586G>A , CM000675.2:g.48045586G>A GRCh38
NC_000013.10:g.48619722G>A , CM000675.1:g.48619722G>A GRCh37
NC_000013.9:g.47517723G>A NCBI36
NG_047021.1:g.13020G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.356-74G>A MANE Select ENSP00000258662.1:n.356-74G>A
ENST00000258662.2:c.356-74G>A ENSP00000258662.1:n.356-74G>A
NM_018283.2:c.356-74G>A NP_060753.1:n.356-74G>A
NM_018283.3:c.356-74G>A NP_060753.1:n.356-74G>A
NR_136687.1:n.536-74G>A
NR_136688.1:n.536-74G>A
NM_018283.4:c.356-74G>A MANE Select NP_060753.1:n.356-74G>A
NR_136687.2:n.377-74G>A
NR_136688.2:n.377-74G>A
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