Canonical Allele Identifier: CA2638808789
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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