Canonical Allele Identifier: CA849430849
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1315332893
gnomAD v3: 8-18388976-C-T
gnomAD v4: 8-18388976-C-T
MyVariant Identifiers: chr8:g.18246486C>T (hg19) chr8:g.18388976C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18388976C>T , CM000670.2:g.18388976C>T GRCh38
NC_000008.10:g.18246486C>T , CM000670.1:g.18246486C>T GRCh37
NC_000008.9:g.18290766C>T NCBI36
NG_012246.1:g.2732C>T

Transcript Alleles

HGVS Amino-acid Change
XM_017012938.1:c.-7+1940C>T XP_016868427.1:n.-7+1940C>T
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