Canonical Allele Identifier: CA291647220
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Linked Data

dbSNP Id: rs896895774
gnomAD v3: 17-51153552-G-T
gnomAD v4: 17-51153552-G-T
MyVariant Identifiers: chr17:g.49230913G>T (hg19) chr17:g.51153552G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153552G>T , CM000679.2:g.51153552G>T GRCh38
NC_000017.10:g.49230913G>T , CM000679.1:g.49230913G>T GRCh37
NC_000017.9:g.46585912G>T NCBI36
NG_021169.1:g.4994G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393196.7:c.-115G>T (NME1) ENSP00000376892.3:n.-115G>T
NM_001018136.2:c.-115G>T (NME1-NME2) NP_001018146.1:n.-115G>T
NR_037149.1:n.17G>T (NME1-NME2)
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