Canonical Allele Identifier: CA2638808786
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153542T>C , CM000679.2:g.51153542T>C GRCh38
NC_000017.10:g.49230903T>C , CM000679.1:g.49230903T>C GRCh37
NC_000017.9:g.46585902T>C NCBI36
NG_021169.1:g.4984T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393196.7:c.-125T>C (NME1) ENSP00000376892.3:n.-125T>C
NM_001018136.2:c.-125T>C (NME1-NME2) NP_001018146.1:n.-125T>C
NR_037149.1:n.7T>C (NME1-NME2)