Canonical Allele Identifier: CA173518479
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs996319496
gnomAD v3: 8-18388888-A-G
gnomAD v4: 8-18388888-A-G
MyVariant Identifiers: chr8:g.18246398A>G (hg19) chr8:g.18388888A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18388888A>G , CM000670.2:g.18388888A>G GRCh38
NC_000008.10:g.18246398A>G , CM000670.1:g.18246398A>G GRCh37
NC_000008.9:g.18290678A>G NCBI36
NG_012246.1:g.2644A>G

Transcript Alleles

HGVS Amino-acid Change
XM_017012938.1:c.-7+1852A>G XP_016868427.1:n.-7+1852A>G
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