Canonical Allele Identifier: CA12545189
Gene: NAMPT HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.106285885C>A
GRCh37 chr7:g.105926331C>A
gnomAD v2:
7:105926331 C / A
gnomAD v3:
7:106285885 C / A
gnomAD v4:
chr7-106285885-C-A
Joint Max Group AF 0.9761155 (EAS)
Genomes Max Group AF 0.97611051 (EAS)
Exomes Max Group AF 0.55689846 (NFE)
dbSNP:
9770242
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.106285885C>A , CM000669.2:g.106285885C>A GRCh38
NC_000007.13:g.105926331C>A , CM000669.1:g.105926331C>A GRCh37
NC_000007.12:g.105713567C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424768.2:c.-442G>T ENSP00000390591.2:n.-442G>T
ENST00000681255.1:c.-392G>T ENSP00000506129.1:n.-392G>T
ENST00000424768.1:c.-442G>T ENSP00000390591.1:n.-442G>T
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