Canonical Allele Identifier: CA849430823
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1478602130
MyVariant Identifiers: chr8:g.18246466G>C (hg19) chr8:g.18388956G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18388956G>C , CM000670.2:g.18388956G>C GRCh38
NC_000008.10:g.18246466G>C , CM000670.1:g.18246466G>C GRCh37
NC_000008.9:g.18290746G>C NCBI36
NG_012246.1:g.2712G>C

Transcript Alleles

HGVS Amino-acid Change
XM_017012938.1:c.-7+1920G>C XP_016868427.1:n.-7+1920G>C
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