Canonical Allele Identifier: CA2638808788
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Linked Data

gnomAD v4: 17-51153544-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153544C>A , CM000679.2:g.51153544C>A GRCh38
NC_000017.10:g.49230905C>A , CM000679.1:g.49230905C>A GRCh37
NC_000017.9:g.46585904C>A NCBI36
NG_021169.1:g.4986C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393196.7:c.-123C>A (NME1) ENSP00000376892.3:n.-123C>A
NM_001018136.2:c.-123C>A (NME1-NME2) NP_001018146.1:n.-123C>A
NR_037149.1:n.9C>A (NME1-NME2)
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