Canonical Allele Identifier: CA8891354
Gene: NAPG HGNC NCBI
COSMIC:
COSN6663275 (not active)
MyVariant.info:
GRCh38 chr18:g.10526190A>G
GRCh37 chr18:g.10526187A>G
gnomAD v2:
18:10526187 A / G
gnomAD v3:
18:10526190 A / G
gnomAD v4:
chr18-10526190-A-G
Joint Max Group AF 0.49749387 (EAS)
Genomes Max Group AF 0.41923712 (EAS)
Exomes Max Group AF 0.50663073 (EAS)
dbSNP:
2290279
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10526190A>G , CM000680.2:g.10526190A>G GRCh38
NC_000018.9:g.10526187A>G , CM000680.1:g.10526187A>G GRCh37
NC_000018.8:g.10516187A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000322897.11:c.56+32A>G MANE Select ENSP00000324628.6:n.56+32A>G
ENST00000322897.10:c.56+32A>G ENSP00000324628.6:n.56+32A>G
ENST00000580224.5:c.56+32A>G ENSP00000463265.1:n.56+32A>G
ENST00000580483.5:c.56+32A>G ENSP00000464496.1:n.56+32A>G
ENST00000580746.1:n.54+32A>G
ENST00000582978.5:n.57+32A>G
NM_003826.2:c.56+32A>G NP_003817.1:n.56+32A>G
XM_011525755.1:c.56+32A>G XP_011524057.1:n.56+32A>G
NM_003826.3:c.56+32A>G MANE Select NP_003817.1:n.56+32A>G
Search 100 bp 5'
Search 100 bp 3'