Canonical Allele Identifier: CA849430890

Gene: NAT2

Linked Data

• dbSNP Id: rs1484956814
• gnomAD v3: 8-18389063-C-T
• gnomAD v4: 8-18389063-C-T
• MyVariant Identifiers: chr8:g.18246573C>T (hg19) ; chr8:g.18389063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18389063C>T , CM000670.2:g.18389063C>T	GRCh38
NC_000008.10:g.18246573C>T , CM000670.1:g.18246573C>T	GRCh37
NC_000008.9:g.18290853C>T	NCBI36
NG_012246.1:g.2819C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017012938.1:c.-7+2027C>T	XP_016868427.1:n.-7+2027C>T