Canonical Allele Identifier: CA849430807
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1327888449
gnomAD v3: 8-18388921-G-A
gnomAD v4: 8-18388921-G-A
MyVariant Identifiers: chr8:g.18246431G>A (hg19) chr8:g.18388921G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18388921G>A , CM000670.2:g.18388921G>A GRCh38
NC_000008.10:g.18246431G>A , CM000670.1:g.18246431G>A GRCh37
NC_000008.9:g.18290711G>A NCBI36
NG_012246.1:g.2677G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017012938.1:c.-7+1885G>A XP_016868427.1:n.-7+1885G>A
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