Canonical Allele Identifier: CA2638808802
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Linked Data

gnomAD v4: 17-51153557-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153557G>A , CM000679.2:g.51153557G>A GRCh38
NC_000017.10:g.49230918G>A , CM000679.1:g.49230918G>A GRCh37
NC_000017.9:g.46585917G>A NCBI36
NG_021169.1:g.4999G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393196.7:c.-110G>A (NME1) ENSP00000376892.3:n.-110G>A
NM_001018136.2:c.-110G>A (NME1-NME2) NP_001018146.1:n.-110G>A
NR_037149.1:n.22G>A (NME1-NME2)
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