Canonical Allele Identifier: CA370635636

Gene: NAT2

Linked Data

• dbSNP Id: rs1800767636
• MyVariant Identifiers: chr8:g.18257835C>G (hg19) ; chr8:g.18400325C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400325C>G , CM000670.2:g.18400325C>G	GRCh38
NC_000008.10:g.18257835C>G , CM000670.1:g.18257835C>G	GRCh37
NC_000008.9:g.18302115C>G	NCBI36
NG_012246.1:g.14081C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.322C>G MANE Select	ENSP00000286479.3:p.Leu108Val
ENST00000286479.3:c.322C>G	ENSP00000286479.3:p.Leu108Val
ENST00000520116.1:c.-57-12C>G	ENSP00000428416.1:n.-57-12C>G
NM_000015.2:c.322C>G	NP_000006.2:p.Leu108Val
XM_011544358.1:c.322C>G	XP_011542660.1:p.Leu108Val
XM_017012938.1:c.322C>G	XP_016868427.1:p.Leu108Val
NM_000015.3:c.322C>G MANE Select	NP_000006.2:p.Leu108Val