Canonical Allele Identifier: CA849430946
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1165005160
MyVariant Identifiers: chr8:g.18246668G>A (hg19) chr8:g.18389158G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18389158G>A , CM000670.2:g.18389158G>A GRCh38
NC_000008.10:g.18246668G>A , CM000670.1:g.18246668G>A GRCh37
NC_000008.9:g.18290948G>A NCBI36
NG_012246.1:g.2914G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017012938.1:c.-7+2122G>A XP_016868427.1:n.-7+2122G>A
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