Canonical Allele Identifier: CA2638808798
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153551G>T , CM000679.2:g.51153551G>T GRCh38
NC_000017.10:g.49230912G>T , CM000679.1:g.49230912G>T GRCh37
NC_000017.9:g.46585911G>T NCBI36
NG_021169.1:g.4993G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393196.7:c.-116G>T (NME1) ENSP00000376892.3:n.-116G>T
NM_001018136.2:c.-116G>T (NME1-NME2) NP_001018146.1:n.-116G>T
NR_037149.1:n.16G>T (NME1-NME2)