Canonical Allele Identifier: CA370636166

Gene: NAT2

Linked Data

• dbSNP Id: rs1800773062
• gnomAD v3: 8-18400568-A-G
• gnomAD v4: 8-18400568-A-G
• MyVariant Identifiers: chr8:g.18258078A>G (hg19) ; chr8:g.18400568A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400568A>G , CM000670.2:g.18400568A>G	GRCh38
NC_000008.10:g.18258078A>G , CM000670.1:g.18258078A>G	GRCh37
NC_000008.9:g.18302358A>G	NCBI36
NG_012246.1:g.14324A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000286479.4:c.565A>G MANE Select	ENSP00000286479.3:p.Ile189Val
ENST00000286479.3:c.565A>G	ENSP00000286479.3:p.Ile189Val
ENST00000520116.1:c.175A>G	ENSP00000428416.1:p.Ile59Val
NM_000015.2:c.565A>G	NP_000006.2:p.Ile189Val
XM_011544358.1:c.565A>G	XP_011542660.1:p.Ile189Val
XM_017012938.1:c.565A>G	XP_016868427.1:p.Ile189Val
NM_000015.3:c.565A>G MANE Select	NP_000006.2:p.Ile189Val