Canonical Allele Identifier: CA772870746
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Linked Data

dbSNP Id: rs1329961781
gnomAD v4: 17-51153545-G-C
MyVariant Identifiers: chr17:g.49230906G>C (hg19) chr17:g.51153545G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153545G>C , CM000679.2:g.51153545G>C GRCh38
NC_000017.10:g.49230906G>C , CM000679.1:g.49230906G>C GRCh37
NC_000017.9:g.46585905G>C NCBI36
NG_021169.1:g.4987G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393196.7:c.-122G>C (NME1) ENSP00000376892.3:n.-122G>C
NM_001018136.2:c.-122G>C (NME1-NME2) NP_001018146.1:n.-122G>C
NR_037149.1:n.10G>C (NME1-NME2)
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